Canonical Allele Identifier: PA645477735
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285159
ClinVar RCV Id: RCV000725599 RCV001495704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Gly1492Ser
CA1707026
NM_001130987.2:c.4474G>A