Canonical Allele Identifier: PA2825759189
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 497848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Arg1101Cys
CA1706513
NM_001130981.2:c.3301C>T