Canonical Allele Identifier: PA2825756590
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 283977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Arg825Gln
CA1706183
NM_001130980.2:c.2474G>A