Canonical Allele Identifier: PA916077056
Gene: FXN HGNC NCBI

Linked Data

ClinVar Variation Id: 264451
ClinVar RCV Id: RCV000507170 RCV000852582 RCV002311184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852090.1:p.Arg40Cys
CA10587675
NM_181425.3:c.118C>T