Canonical Allele Identifier: PA237075
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 191617
ClinVar RCV Id: RCV000171886 RCV002390410 RCV003105808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Glu468Asp
CA237073
NM_001927.4:c.1404A>C
CA350699198
NM_001927.4:c.1404A>T