Allele Registry

Canonical Allele Identifier: PA101306

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001860

RCV000185577

RCV001387555

ClinVar Variation:

1787

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Arg347His	CA115184 NM_000102.4:c.1040G>A