Canonical Allele Identifier: PA2580108398
Gene: HSD11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2035909
ClinVar RCV Id: RCV002894563 RCV003167859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000187.3:p.Leu395Pro
CA8110828
NM_000196.4:c.1184T>C