Allele Registry

Canonical Allele Identifier: PA112133

Gene: FXN HGNC NCBI

ClinVar RCV:

RCV001353170

RCV003928855

ClinVar Variation:

1048603

HGVS (amino-acid)	Matching Registered Transcripts
NP_000135.2:p.Arg165Cys	CA193982463 NM_000144.5:c.493C>T