Canonical Allele Identifier: PA105520
Gene: HSD11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000187.3:p.Arg208His
CA121882
NM_000196.4:c.623G>A