Canonical Allele Identifier: PA2826069572
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 280110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.Pro524Leu
CA10603390
NM_001170634.1:c.1571C>T