Canonical Allele Identifier: PA2828917410
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 956598
ClinVar RCV Id: RCV001229432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.His351Gln
CA350698500
NM_001382713.1:c.1053T>A
CA350698503
NM_001382713.1:c.1053T>G