Canonical Allele Identifier: PA645497858
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 411147

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Gln131Lys
CA2125062
NM_001927.4:c.391C>A