Canonical Allele Identifier: PA2825063962
Gene: FXN HGNC NCBI

Linked Data

ClinVar Variation Id: 2500463
ClinVar RCV Id: RCV003225375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000135.2:p.Lys135Arg
CA5072747
NM_000144.5:c.404A>G