Canonical Allele Identifier: PA2825770763
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 452293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Ala1960Val
CA1707565
NM_001130986.2:c.5879C>T