Canonical Allele Identifier: PA2827179493
Gene: DSE HGNC NCBI
ClinVar RCV:
RCV000515451
ClinVar Variation:
446171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309867.1:p.Arg267Gly
CA365392721
NM_001322938.2:c.799A>G