Allele Registry

Canonical Allele Identifier: PA115197

Gene: CYP17A1 HGNC NCBI

ClinVar Allele:

16839

ClinVar RCV:

RCV000001873

ClinVar Variation:

1800

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Tyr201Asn	CA115196 NM_000102.4:c.601T>A