Canonical Allele Identifier: PA2825762763
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 283977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Arg809Gln
CA1706183
NM_001130983.2:c.2426G>A