Canonical Allele Identifier: PA915972686
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 317128
ClinVar RCV Id: RCV000318244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093243.1:p.Asp39His
CA10647402
NM_001099773.2:c.115G>C