Canonical Allele Identifier: PA645387633
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 317123
ClinVar RCV Id: RCV000358686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000772.2:p.Asp401Asn
CA10646601
NM_000781.3:c.1201G>A