Canonical Allele Identifier: PA916077100
Gene: FXN HGNC NCBI

Linked Data

ClinVar Variation Id: 549677
ClinVar RCV Id: RCV000664219
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852090.1:p.Asn146Lys
CA193393064
NM_181425.3:c.438C>G
CA373530847
NM_181425.3:c.438C>A