Canonical Allele Identifier: PA2828915261
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_001369637.1:p.His440Gln
CA350698500
NM_001382708.1:c.1320T>A
CA350698503
NM_001382708.1:c.1320T>G