Allele Registry

Canonical Allele Identifier: PA121932

Gene: HSD3B2 HGNC NCBI

ClinVar RCV:

RCV000012973

RCV001233258

ClinVar Variation:

12190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159592.1:p.Glu142Lys	CA121931 NM_001166120.2:c.424G>A