Allele Registry

Canonical Allele Identifier: PA126285

Gene: FUS HGNC NCBI

ClinVar RCV:

RCV000017608

ClinVar Variation:

16221

HGVS (amino-acid)	Matching Registered Transcripts
NP_004951.1:p.His517Gln	CA126283 NM_004960.4:c.1551C>G CA395677356 NM_004960.4:c.1551C>A