Canonical Allele Identifier: PA2828916108
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1436615
ClinVar RCV Id: RCV001962629 RCV002407124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Ser6Trp
CA350682089
NM_001382711.1:c.17C>G