Allele Registry

Canonical Allele Identifier: PA2826069562

Gene: FUS HGNC NCBI

ClinVar RCV:

RCV000017615

RCV001362689

ClinVar Variation:

16228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001164105.1:p.Arg523Trp	CA257447 NM_001170634.1:c.1567A>T