Canonical Allele Identifier: PA2825694258
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 582986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Thr1037Arg
CA49746708
NM_001130455.2:c.3110C>G