Canonical Allele Identifier: PA658678106
Gene: HSD11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447526
ClinVar RCV Id: RCV000518271 RCV002476043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000187.3:p.Arg147His
CA8110617
NM_000196.4:c.440G>A