Canonical Allele Identifier: PA645388687
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 427141
ClinVar RCV Id: RCV000489255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004951.1:p.Met254Val
CA8023782
NM_004960.4:c.760A>G