Canonical Allele Identifier: PA2828916042
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2102249
ClinVar RCV Id: RCV003037634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Ala380Asp
CA350694984
NM_001382710.1:c.1139C>A