Canonical Allele Identifier: PA658678104
Gene: HSD11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447525
ClinVar RCV Id: RCV000517382 RCV001570971 RCV000995564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000187.3:p.Gly89Asp
CA396277387
NM_000196.4:c.266G>A