Canonical Allele Identifier: PA2825765258
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 582986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Thr1023Arg
CA49746708
NM_001130984.2:c.3068C>G