Canonical Allele Identifier: PA915984524
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 650787
ClinVar RCV Id: RCV000806009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004951.1:p.Gln519Glu
CA395677387
NM_004960.4:c.1555C>G