Canonical Allele Identifier: PA1139699051
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 929767
ClinVar RCV Id: RCV001270218 RCV003323811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Val215Gly
CA377939768
NM_000102.4:c.644T>G