Canonical Allele Identifier: PA2580301620
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 2068354
ClinVar RCV Id: RCV002971104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004951.1:p.Gln179His
CA395669543
NM_004960.4:c.537A>C
CA395669546
NM_004960.4:c.537A>T