Allele Registry

Canonical Allele Identifier: PA2826069532

Gene: FUS HGNC NCBI

ClinVar RCV:

RCV000489101

RCV002526045

ClinVar Variation:

427191

HGVS (amino-acid)	Matching Registered Transcripts
NP_001164105.1:p.His516Arg	CA395677337 NM_001170634.1:c.1547A>G