Canonical Allele Identifier: PA2825474396
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 391864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001074445.1:p.Ile120Thr
CA3969503
NM_001080976.3:c.359T>C