Canonical Allele Identifier: PA2825063963
Gene: FXN HGNC NCBI

Linked Data

ClinVar Variation Id: 2461756
ClinVar RCV Id: RCV003184856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000135.2:p.Gly138Arg
CA5072748
NM_000144.5:c.412G>A
CA373530793
NM_000144.5:c.412G>C