Canonical Allele Identifier: PA2825750061
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 242418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Arg1024Gln
CA1706448
NM_001130977.2:c.3071G>A