Canonical Allele Identifier: PA645387566
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 317134
ClinVar RCV Id: RCV000345392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000772.2:p.Arg29His
CA7656692
NM_000781.3:c.86G>A