Allele Registry

Canonical Allele Identifier: PA212940

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000012882

RCV000761442

ClinVar Variation:

12100

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Glu115_Leu116del	CA212939 NM_000196.4:c.343_348del