Canonical Allele Identifier: PA2828916281
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1991980
ClinVar RCV Id: RCV002776453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Leu143Arg
CA350686092
NM_001382711.1:c.428T>G