Canonical Allele Identifier: PA2828915474
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1740814
ClinVar RCV Id: RCV002328465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Thr149Arg
CA350686276
NM_001382709.1:c.446C>G