Canonical Allele Identifier: PA2828915017
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1310579
ClinVar RCV Id: RCV001767693 RCV002488572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Gln165Arg
CA350686649
NM_001382708.1:c.494A>G