Allele Registry

Canonical Allele Identifier: PA101376

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001858

RCV000255053

RCV000501502

RCV003114170

ClinVar Variation:

1785

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Arg96Trp	CA115183 NM_000102.4:c.286C>T