Allele Registry

Canonical Allele Identifier: PA2825063968

Gene: FXN HGNC NCBI

ClinVar RCV:

RCV001663613

ClinVar Variation:

1256271

HGVS (amino-acid)	Matching Registered Transcripts
NP_000135.2:p.Leu156Pro	CA5072757 NM_000144.5:c.467T>C