Canonical Allele Identifier: PA105610
Gene: HSD11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 31131
ClinVar RCV Id: RCV000024127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000187.3:p.Tyr338His
CA129702
NM_000196.4:c.1012T>C