Canonical Allele Identifier: PA2829466836
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 283977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Arg808Gln
CA1706183
NM_003494.4:c.2423G>A