Allele Registry

Canonical Allele Identifier: PA101396

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV000001866

ClinVar Variation:

1793

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Asp116Val	CA115190 NM_000102.4:c.347A>T