Allele Registry

Canonical Allele Identifier: PA2829594055

Gene: HSD11B1 HGNC NCBI

ClinVar RCV:

RCV000024294

ClinVar Variation:

31588

HGVS (amino-acid)	Matching Registered Transcripts
NP_005516.1:p.Arg137Cys	CA213398 NM_005525.4:c.409C>T