Canonical Allele Identifier: PA916077098
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_852090.1:p.Gly130Val
CA252966
NM_181425.3:c.389G>T