Canonical Allele Identifier: PA101296
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1794
ClinVar RCV Id: RCV000001867 RCV001804711 RCV002221463 RCV003555893 RCV003988818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Arg347Cys
CA115191
NM_000102.4:c.1039C>T