Canonical Allele Identifier: PA2825760177
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 452293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Ala2011Val
CA1707565
NM_001130981.2:c.6032C>T