Canonical Allele Identifier: PA2828915237
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2090670
ClinVar RCV Id: RCV002991421
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Glu411Asp
CA350695096
NM_001382708.1:c.1233G>C
CA350695098
NM_001382708.1:c.1233G>T