Canonical Allele Identifier: PA2828915478
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2922965
ClinVar RCV Id: RCV003788131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Glu153Asp
CA350686378
NM_001382709.1:c.459G>C
CA350686382
NM_001382709.1:c.459G>T