Canonical Allele Identifier: PA2825769746
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2441152
ClinVar RCV Id: RCV003146981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Gln1039Lys
CA347217130
NM_001130986.2:c.3115C>A