Canonical Allele Identifier: PA2826069364
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 2922331
ClinVar RCV Id: RCV003785545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.Asn294Ser
CA395672235
NM_001170634.1:c.881A>G