Canonical Allele Identifier: PA645498538
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 411144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Ala462Glu
CA16610673
NM_001927.4:c.1385_1386delinsAG