Allele Registry

Canonical Allele Identifier: PA101492

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001852

RCV000288112

RCV000763211

RCV003914797

ClinVar Variation:

1780

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Ser106Pro	CA115179 NM_000102.4:c.316T>C