Canonical Allele Identifier: PA2827179136
Gene: DSE HGNC NCBI
ClinVar RCV:
RCV001362844
ClinVar Variation:
1054354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309866.1:p.Cys18Tyr
CA3969445
NM_001322937.2:c.53G>A