Allele Registry

Canonical Allele Identifier: PA121934

Gene: HSD3B2 HGNC NCBI

ClinVar RCV:

RCV000012974

RCV002271368

ClinVar Variation:

12191

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159592.1:p.Pro222Thr	CA121933 NM_001166120.2:c.664C>A