Canonical Allele Identifier: PA2825749030
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 579361
ClinVar RCV Id: RCV000702622
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Val68Met
CA1705254
NM_001130977.2:c.202G>A