Canonical Allele Identifier: PA2827179209
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 88848
ClinVar RCV Id: RCV000074436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309866.1:p.Ser268Leu
CA145364
NM_001322937.2:c.803C>T