Canonical Allele Identifier: PA2828915051
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 3221932
ClinVar RCV Id: RCV004511255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Gln188Arg
CA350687136
NM_001382708.1:c.563A>G