Canonical Allele Identifier: PA2825752712
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1932275
ClinVar RCV Id: RCV002649399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124450.1:p.Asn1373Lys
CA49779104
NM_001130978.2:c.4119C>A
CA347228694
NM_001130978.2:c.4119C>G