Canonical Allele Identifier: PA2825766419
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 896081
ClinVar RCV Id: RCV001138530
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Leu2083Val
CA347227885
NM_001130984.2:c.6247C>G