Canonical Allele Identifier: PA2826069532
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 427191
ClinVar RCV Id: RCV000489101 RCV002526045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.His516Arg
CA395677337
NM_001170634.1:c.1547A>G