Canonical Allele Identifier: PA915972691
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29625
ClinVar RCV Id: RCV000022465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093243.1:p.Leu64Pro
CA128509
NM_001099773.2:c.191T>C