Canonical Allele Identifier: PA645387600
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 317128
ClinVar RCV Id: RCV000318244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000772.2:p.Asp197His
CA10647402
NM_000781.3:c.589G>C