Canonical Allele Identifier: PA2828917427
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2922193
ClinVar RCV Id: RCV003785407 RCV004374385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Thr373Ile
CA350699035
NM_001382713.1:c.1118C>T