Allele Registry

Canonical Allele Identifier: PA121938

Gene: HSD3B2 HGNC NCBI

ClinVar RCV:

RCV000012977

ClinVar Variation:

12194

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159592.1:p.Pro341Leu	CA121937 NM_001166120.2:c.1022C>T