Canonical Allele Identifier: PA2828917019
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1285006
ClinVar RCV Id: RCV001703364 RCV004039959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Arg436Ser
CA65986916
NM_001382712.1:c.1308G>C
CA350698409
NM_001382712.1:c.1308G>T