Canonical Allele Identifier: PA2827179421
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 1054354
ClinVar RCV Id: RCV001362844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309867.1:p.Cys18Tyr
CA3969445
NM_001322938.2:c.53G>A