Canonical Allele Identifier: PA2825764808
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1504301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Met613Val
CA1705982
NM_001130984.2:c.1837A>G