Allele Registry

Canonical Allele Identifier: PA112154

Gene: FXN HGNC NCBI

ClinVar RCV:

RCV000004189

RCV000992016

ClinVar Variation:

3982

HGVS (amino-acid)	Matching Registered Transcripts
NP_000135.2:p.Gly130Val	CA252966 NM_000144.5:c.389G>T