Allele Registry

Canonical Allele Identifier: PA105562

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000012883

RCV002512996

ClinVar Variation:

12101

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Asp223Asn	CA121888 NM_000196.4:c.667G>A