Canonical Allele Identifier: PA2580301688
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 2018615
ClinVar RCV Id: RCV002862117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004951.1:p.Arg522Ser
CA395677477
NM_004960.4:c.1566G>C
CA395677482
NM_004960.4:c.1566G>T