Canonical Allele Identifier: PA2825694718
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2199498
ClinVar RCV Id: RCV002659668
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Glu1295Lys
CA1706801
NM_001130455.2:c.3883G>A