Allele Registry

Canonical Allele Identifier: PA101430

Gene: CYP17A1 HGNC NCBI

ClinVar Allele:

16831

ClinVar RCV:

RCV000001865

ClinVar Variation:

1792

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Phe114Val	CA115189 NM_000102.4:c.340T>G