Canonical Allele Identifier: PA2825747823
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2441152
ClinVar RCV Id: RCV003146981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Gln1038Lys
CA347217130
NM_001130976.2:c.3112C>A