Canonical Allele Identifier: PA2826069433
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 37069
ClinVar RCV Id: RCV000030718 RCV000711709 RCV000765290 RCV001847624 RCV002381274 RCV003407373 RCV003993752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.Pro430Leu
CA130060
NM_001170634.1:c.1289C>T