Canonical Allele Identifier: PA891852132
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 575369
ClinVar RCV Id: RCV000697561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Arg163Gln
CA350686609
NM_001927.4:c.488G>A