Canonical Allele Identifier: PA2828916000
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2935423
ClinVar RCV Id: RCV003791077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Asp342His
CA350694143
NM_001382710.1:c.1024G>C