Canonical Allele Identifier: PA259636
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 29708
ClinVar RCV Id: RCV000022557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004951.1:p.Gly206Ser
CA259634
NM_004960.4:c.616G>A