Canonical Allele Identifier: PA110552
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29625
ClinVar RCV Id: RCV000022465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000772.2:p.Leu222Pro
CA128509
NM_000781.3:c.665T>C