Canonical Allele Identifier: PA2828915825
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2949962
ClinVar RCV Id: RCV003807320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Arg146Gly
CA350686181
NM_001382710.1:c.436C>G