Canonical Allele Identifier: PA913197327
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 626714
ClinVar RCV Id: RCV000770173 RCV001352202 RCV002487571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Arg415Gln
CA350695133
NM_001927.4:c.1244G>A