Allele Registry

Canonical Allele Identifier: PA2499229590

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV001519942

RCV002501825

ClinVar Variation:

1169108

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Val273Met	CA8110760 NM_000196.4:c.817G>A