Canonical Allele Identifier: PA658655369
Gene: DSE HGNC NCBI
ClinVar RCV:
RCV000074436
ClinVar Variation:
88848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037484.1:p.Ser268Leu
CA145364
NM_013352.4:c.803C>T