Allele Registry

Canonical Allele Identifier: PA112168

Gene: FXN HGNC NCBI

ClinVar RCV:

RCV000711718

ClinVar Variation:

585891

HGVS (amino-acid)	Matching Registered Transcripts
NP_000135.2:p.Leu106Ser	CA193385325 NM_000144.5:c.317T>C