Canonical Allele Identifier: PA2825757269
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2441141
ClinVar RCV Id: RCV003146970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Val1406Met
CA347228972
NM_001130980.2:c.4216G>A