Canonical Allele Identifier: PA2825757771
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2885593
ClinVar RCV Id: RCV003735522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Asp1854His
CA347223076
NM_001130980.2:c.5560G>C