Canonical Allele Identifier: PA2828915439
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 955639
ClinVar RCV Id: RCV001228319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Ile123Val
CA2125057
NM_001382709.1:c.367A>G