Canonical Allele Identifier: PA2826075816
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 430234
ClinVar RCV Id: RCV000493726 RCV001118682 RCV002527105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164408.1:p.Pro455Leu
CA395675519
NM_001170937.1:c.1364C>T