Allele Registry

Canonical Allele Identifier: PA3057575748

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000012878

RCV005089240

ClinVar Variation:

12097

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Arg337_Tyr338delinsHis	CA121883 NM_000196.4:c.1010_1012del