Allele Registry

Canonical Allele Identifier: PA916077097

Gene: FXN HGNC NCBI

ClinVar RCV:

RCV000029175

ClinVar Variation:

35514

HGVS (amino-acid)	Matching Registered Transcripts
NP_852090.1:p.Asp124_Ser126delinsValHisLeuGluAspThr	CA10575562 NM_181425.3:c.371_376delinsTACACCTTGAGGACA