Allele Registry

Canonical Allele Identifier: PA101454

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001864

ClinVar Variation:

1791

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Phe93Cys	CA115188 NM_000102.4:c.278T>G