Allele Registry

Canonical Allele Identifier: PA101485

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001872

RCV001220851

RCV001831506

ClinVar Variation:

1799

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Pro428Leu	CA115195 NM_000102.4:c.1283C>T