Canonical Allele Identifier: PA2826075644
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 16227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164408.1:p.Arg212Cys
CA130062
NM_001170937.1:c.634C>T