Canonical Allele Identifier: PA2825764729
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2102928
ClinVar RCV Id: RCV003037820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Leu529Val
CA347217508
NM_001130984.2:c.1585C>G