Canonical Allele Identifier: PA645477838
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 287816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Arg2039Gln
CA1707599
NM_001130987.2:c.6116G>A