Canonical Allele Identifier: PA2827180342
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 1054354
ClinVar RCV Id: RCV001362844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309873.1:p.Cys18Tyr
CA3969445
NM_001322944.2:c.53G>A