Allele Registry

Canonical Allele Identifier: PA121928

Gene: HSD3B2 HGNC NCBI

ClinVar RCV:

RCV000012971

ClinVar Variation:

12188

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159592.1:p.Ala10Glu	CA121927 NM_001166120.2:c.29C>A