Allele Registry

Canonical Allele Identifier: PA2825068720

Gene: CYP17A1 HGNC NCBI

ClinVar Allele:

3239518

ClinVar RCV:

RCV004367762

ClinVar Variation:

3079368

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Lys388Glu	CA377938589 NM_000102.4:c.1162A>G