Canonical Allele Identifier: PA098538
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 16223
ClinVar RCV Id: RCV000017610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004951.1:p.Arg518Lys
CA257439
NM_004960.4:c.1553G>A