Canonical Allele Identifier: PA2826075890
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 427191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164408.1:p.His513Arg
CA395677337
NM_001170937.1:c.1538A>G