CYP1A1*2A Allele NG_061374.1:g.11229T>C

HGVS Expressions

  • NG_061374.1:g.11229T>C
  • CYP1A1*2A Allele NG_061374.1:g.11229T>C
  • NC_000015.10:g.74719300A>G
Back to search Result
CTGA Clinical Significance

Benign, Drug Response, Risk factor

Variant Type

Substitution

dbSNP

4646903

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.