Allele Registry

Canonical Allele Identifier: PA2741809154

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV003337809

ClinVar Variation:

2585193

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Trp406Gly	CA377938465 NM_000102.4:c.1216T>G