Canonical Allele Identifier: PA112154
Gene: FXN HGNC NCBI

Linked Data

ClinVar Variation Id: 3982
ClinVar RCV Id: RCV000004189 RCV000992016
JSON-LD

Amino-acid Alleles

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