Canonical Allele Identifier: PA2825753368
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 452293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124450.1:p.Ala1994Val
CA1707565
NM_001130978.2:c.5981C>T