Allele Registry

Canonical Allele Identifier: PA101364

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001875

RCV001067683

RCV002298430

RCV003460404

ClinVar Variation:

1802

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Arg96Gln	CA115200 NM_000102.4:c.287G>A