Allele Registry

Canonical Allele Identifier: PA105510

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000012874

ClinVar Variation:

12093

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Arg208Cys	CA121879 NM_000196.4:c.622C>T