Allele Registry

Canonical Allele Identifier: PA101536

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001871

ClinVar Variation:

1798

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Tyr329Asp	CA115194 NM_000102.4:c.985T>G