• Genetic Testing for Severe Inherited Diseases, NGS
  • Chronic Fatigue Syndrome Diagnostic Panel
  • Familial Adenomatous Polyposis (APC), Sequencing
  • Fibrinogen Antigen
  • Fecal Occult Blood
  • Ki-67
  • Lorazepam, Urine
  • Brucella Culture
  • Protein, Total, Serum
  • Brugada Syndrome Multi-Gene Panel, NGS
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /N-Acetyltransferase 2 (NAT2) Gene Mutation 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

N-Acetyltransferase 2 (NAT2) Gene Mutation Analysis
Medical Test

Methodology
Access to N-Acetyltransferase 2 (NAT2) Gene Mutation Analysis is restricted.