Canonical Allele Identifier: PA2826075919
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 280110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164408.1:p.Pro521Leu
CA10603390
NM_001170937.1:c.1562C>T