Canonical Allele Identifier: PA2828915027
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2006854
ClinVar RCV Id: RCV002837951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Arg173Gly
CA350686826
NM_001382708.1:c.517C>G