Canonical Allele Identifier: PA2825765268
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1491619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Arg1026Gln
CA1706451
NM_001130984.2:c.3077G>A