Canonical Allele Identifier: PA2828914980
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2942772
ClinVar RCV Id: RCV003807938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Ala137Thr
CA350685966
NM_001382708.1:c.409G>A