Canonical Allele Identifier: PA2825758575
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Gly536Arg
CA253913
NM_001130981.2:c.1606G>A
CA347217356
NM_001130981.2:c.1606G>C