Canonical Allele Identifier: PA645388740
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_004951.1:p.His517Arg
CA395677337
NM_004960.4:c.1550A>G