Canonical Allele Identifier: PA2825748570
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Thr1704Pro
CA1707307
NM_001130976.2:c.5110A>C