Canonical Allele Identifier: PA2825762483
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Gly520Arg
CA253913
NM_001130983.2:c.1558G>A
CA347217356
NM_001130983.2:c.1558G>C