Canonical Allele Identifier: PA645477586
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Gly537Arg
CA253913
NM_001130987.2:c.1609G>A
CA347217356
NM_001130987.2:c.1609G>C