Canonical Allele Identifier: PA915975795
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 813988
ClinVar RCV Id: RCV002265924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Glu167Gly
CA350686692
NM_001927.4:c.500A>G