Canonical Allele Identifier: PA2825474436
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 392192
ClinVar RCV Id: RCV000436673 RCV002522675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001074445.1:p.Arg335His
CA3969607
NM_001080976.3:c.1004G>A