• Splicing Factor 3b Subunit B1 (SF3B1) Gene Mutation Analysis
  • 17-Hydroxyprogesterone, Urine
  • Acute Hepatitis Panel
  • Lipoprotein Associated Phospholipase A2 Activity
  • Electrolyte Panel, Urine
  • Dopamine transporter (DAT1) (SLC6A3) Genotyping
  • Mitochondrial Antibody, IgG
  • Williams Syndrome, 7q11.23 Deletion
  • Vitamin B12 and Folate
  • Antinuclear Antibody (ANA) Screen
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /TNNC1 (Troponin C) Gene Mutation Analysis
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

TNNC1 (Troponin C) Gene Mutation Analysis
Medical Test

Diseases (2)
Access to TNNC1 (Troponin C) Gene Mutation Analysis is restricted.