Canonical Allele Identifier: PA2825747797
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 582986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Thr1022Arg
CA49746708
NM_001130976.2:c.3065C>G