Canonical Allele Identifier: PA2825765262
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 661790
ClinVar RCV Id: RCV000819285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.His1024Tyr
CA1706445
NM_001130984.2:c.3070C>T