Canonical Allele Identifier: PA2825759439
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 955680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Glu1311Gly
CA347226584
NM_001130981.2:c.3932A>G