Canonical Allele Identifier: PA2825765851
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285741
ClinVar RCV Id: RCV000306735 RCV000338437 RCV001055238 RCV000406757 RCV001833354 RCV002519192
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Pro1563Ser
CA1707143
NM_001130984.2:c.4687C>T