Canonical Allele Identifier: PA2826069531
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 16221
ClinVar RCV Id: RCV000017608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164105.1:p.His516Gln
CA126283
NM_001170634.1:c.1548C>G
CA395677356
NM_001170634.1:c.1548C>A