Canonical Allele Identifier: PA2826068991
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 447356
ClinVar RCV Id: RCV000517990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.Thr11Ala
CA8023413
NM_001170634.1:c.31A>G