Allele Registry

Canonical Allele Identifier: PA105542

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000012879

ClinVar Variation:

12098

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Arg279Cys	CA121885 NM_000196.4:c.835C>T