Canonical Allele Identifier: PA100591
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 16834
ClinVar RCV Id: RCV000056784 RCV000811753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Thr442Ile
CA217036
NM_001927.4:c.1325C>T