Canonical Allele Identifier: PA2828917089
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 956977
ClinVar RCV Id: RCV001229880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Gly44Val
CA350683193
NM_001382713.1:c.131G>T