Allele Registry

Canonical Allele Identifier: PA115206

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001879

ClinVar Variation:

1806

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Phe453Ser	CA115205 NM_000102.4:c.1358T>C