Allele Registry

Canonical Allele Identifier: PA2580102952

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV003074305

ClinVar Variation:

2145932

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Asp139Asn	CA5669575 NM_000102.4:c.415G>A