Canonical Allele Identifier: PA2828915181
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2178066
ClinVar RCV Id: RCV002588503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Gly361Asp
CA350694085
NM_001382708.1:c.1082G>A