Allele Registry

Canonical Allele Identifier: PA101296

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001867

RCV001804711

RCV002221463

RCV003555893

RCV003988818

ClinVar Variation:

1794

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