Allele Registry

Canonical Allele Identifier: PA105610

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000024127

ClinVar Variation:

31131

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Tyr338His	CA129702 NM_000196.4:c.1012T>C