Allele Registry

Canonical Allele Identifier: PA2580102933

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV002973540

ClinVar Variation:

2351843

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Ala105Val	CA5669593 NM_000102.4:c.314C>T