Canonical Allele Identifier: PA2825765006
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 497312
ClinVar RCV Id: RCV000596941 RCV000817716 RCV001829634
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Arg806Gln
CA1706192
NM_001130984.2:c.2417G>A