Allele Registry

Canonical Allele Identifier: PA105955

Gene: HSD3B2 HGNC NCBI

ClinVar RCV:

RCV000012974

RCV002271368

ClinVar Variation:

12191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000189.1:p.Pro222Thr	CA121933 NM_000198.4:c.664C>A