Canonical Allele Identifier: PA2825760143
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 647886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Ala1977Thr
CA1707553
NM_001130981.2:c.5929G>A