Canonical Allele Identifier: PA2828914951
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2169507
ClinVar RCV Id: RCV003084860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Leu115Ile
CA350685384
NM_001382708.1:c.343C>A