Canonical Allele Identifier: PA2828915052
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2079657
ClinVar RCV Id: RCV002998687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Gln188His
CA350687143
NM_001382708.1:c.564G>C
CA350687146
NM_001382708.1:c.564G>T