Canonical Allele Identifier: PA916026717
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 452829
ClinVar RCV Id: RCV000520971 RCV001853691 RCV004023623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309868.1:p.Arg742Gln
CA3969774
NM_001322939.2:c.2225G>A