Canonical Allele Identifier: PA2828126896
Gene: FTO HGNC NCBI
ClinVar RCV:
RCV000001110
ClinVar Variation:
1055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350826.1:p.Arg290Gln
CA114727
NM_001363897.1:c.869G>A