• Amylase, Body Fluid
  • Heavy Metals Screen, 24 Hour, Urine
  • JAK2 (V617F) Gene Mutation Analysis
  • Factor XIII (F13A1) V34L Genetic Variation Analysis
  • Carcinoembryonic Antigen (CEA), Pancreatic Cyst Fluid
  • Cardiac Ion Channelopathies Multi-Gene Panel, NGS
  • Group A Streptococcus (Streptococcus pyogenes) Rapid with Reflex to Culture
  • Human T-Cell Lymphotropic Virus (HTLV) I/II, Nucleic Acid Detection
  • Ki-67, Immunohistochemistry (IHC)
  • Heparin Induced Antibody
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Factor XIII (F13A1) V34L Genetic Variation Analysis
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Factor XIII (F13A1) V34L Genetic Variation Analysis
Medical Test

Methodology
Access to Factor XIII (F13A1) V34L Genetic Variation Analysis is restricted.
Loading...