Canonical Allele Identifier: PA2826069555
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 2018615
ClinVar RCV Id: RCV002862117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.Arg521Ser
CA395677477
NM_001170634.1:c.1563G>C
CA395677482
NM_001170634.1:c.1563G>T