Canonical Allele Identifier: PA2825750834
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Thr1725Pro
CA1707307
NM_001130977.2:c.5173A>C