Allele Registry

Canonical Allele Identifier: PA115178

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001850

RCV001382543

RCV001826402

ClinVar Variation:

1778

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Phe54del	CA115176 NM_000102.4:c.160_162del