Canonical Allele Identifier: PA121887
Gene: HSD11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12099
ClinVar RCV Id: RCV000012881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000187.3:p.Pro227Leu
CA121886
NM_000196.4:c.680C>T