Canonical Allele Identifier: PA100367
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 66389
ClinVar RCV Id: RCV000056768 RCV000799745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Arg355Pro
CA217005
NM_001927.4:c.1064G>C