Canonical Allele Identifier: PA2828916119
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1405121
ClinVar RCV Id: RCV001903577 RCV003146333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Arg15Ser
CA16622111
NM_001382711.1:c.43C>A