Allele Registry

Canonical Allele Identifier: PA101326

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001869

RCV000810182

RCV001831505

RCV003114171

RCV003415624

ClinVar Variation:

1796

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Arg362Cys	CA115192 NM_000102.4:c.1084C>T