Canonical Allele Identifier: PA2826069240
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 16227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.Arg215Cys
CA130062
NM_001170634.1:c.643C>T