Canonical Allele Identifier: PA2828917021
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1709013
ClinVar RCV Id: RCV002288297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Ser438Tyr
CA350698438
NM_001382712.1:c.1313C>A