Allele Registry

Canonical Allele Identifier: PA101316

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001861

RCV001804710

RCV001851566

RCV003466780

ClinVar Variation:

1788

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Arg358Gln	CA115185 NM_000102.4:c.1073G>A