Canonical Allele Identifier: PA2828915960
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1677711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Asn288Lys
CA350691670
NM_001382710.1:c.864C>A
CA350691672
NM_001382710.1:c.864C>G