Canonical Allele Identifier: PA2828916586
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2933947
ClinVar RCV Id: RCV003793505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Val11Leu
CA350682207
NM_001382712.1:c.31G>T
CA350682208
NM_001382712.1:c.31G>C