Allele Registry

Canonical Allele Identifier: PA213399

Gene: HSD11B1 HGNC NCBI

ClinVar RCV:

RCV000024294

ClinVar Variation:

31588

HGVS (amino-acid)	Matching Registered Transcripts
NP_861420.1:p.Arg137Cys	CA213398 NM_181755.3:c.409C>T