Canonical Allele Identifier: PA2825755463
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Arg1827Trp
CA1707403
NM_001130979.2:c.5479C>T