Canonical Allele Identifier: PA2828916468
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1989564
ClinVar RCV Id: RCV002795732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Gln357His
CA350694135
NM_001382711.1:c.1071G>C
CA350694138
NM_001382711.1:c.1071G>T