Canonical Allele Identifier: PA2825694275
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1491619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Arg1040Gln
CA1706451
NM_001130455.2:c.3119G>A