Canonical Allele Identifier: PA098672
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 280110
ClinVar RCV Id: RCV000381069 RCV001069729 RCV001095439 RCV003401225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004951.1:p.Pro525Leu
CA10603390
NM_004960.4:c.1574C>T