Canonical Allele Identifier: PA2826075633
Gene: FUS HGNC NCBI
ClinVar Allele:
38663
ClinVar RCV:
RCV000022557
ClinVar Variation:
29708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164408.1:p.Gly202Ser
CA259634
NM_001170937.1:c.604G>A