Canonical Allele Identifier: PA916077049
Gene: FXN HGNC NCBI

Linked Data

ClinVar Variation Id: 618139
ClinVar RCV Id: RCV000756192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852090.1:p.Leu12Val
CA373527297
NM_181425.3:c.34C>G