Canonical Allele Identifier: PA2499248935
Gene: DSE HGNC NCBI
ClinVar RCV:
RCV001362844
ClinVar Variation:
1054354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309868.1:p.Cys37Tyr
CA3969445
NM_001322939.2:c.110G>A