Allele Registry

Canonical Allele Identifier: PA101518

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001870

RCV001851567

RCV003466781

ClinVar Variation:

1797

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Trp406Arg	CA115193 NM_000102.4:c.1216T>C CA377938466 NM_000102.4:c.1216T>A