Canonical Allele Identifier: PA2826069543
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 16222
ClinVar RCV Id: RCV000017609 RCV000703284 RCV002472932 RCV003421921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.Arg520Gly
CA257437
NM_001170634.1:c.1558C>G