Allele Registry

Canonical Allele Identifier: PA101465

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001856

RCV003555891

ClinVar Variation:

1783

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Pro342Thr	CA115182 NM_000102.4:c.1024C>A