Canonical Allele Identifier: PA2828915661
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1461140
ClinVar RCV Id: RCV001965707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Arg15Cys
CA2125008
NM_001382710.1:c.43C>T