Allele Registry

Canonical Allele Identifier: PA105520

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000012877

RCV002508774

ClinVar Variation:

12096

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Arg208His	CA121882 NM_000196.4:c.623G>A