Canonical Allele Identifier: PA2825766002
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 217227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Arg1701Trp
CA279083
NM_001130984.2:c.5101C>T