Canonical Allele Identifier: PA2828916310
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1499240
ClinVar RCV Id: RCV002010521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Glu167Asp
CA350686698
NM_001382711.1:c.501G>C
CA350686701
NM_001382711.1:c.501G>T