Canonical Allele Identifier: PA2826075626
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 956175
ClinVar RCV Id: RCV001228930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164408.1:p.Gly187Ser
CA280594678
NM_001170937.1:c.559G>A