Allele Registry

Canonical Allele Identifier: PA105962

Gene: HSD3B2 HGNC NCBI

ClinVar RCV:

RCV000012977

ClinVar Variation:

12194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000189.1:p.Pro341Leu	CA121937 NM_000198.4:c.1022C>T