Canonical Allele Identifier: PA2828127521
Gene: FTO HGNC NCBI
ClinVar RCV:
RCV000001110
ClinVar Variation:
1055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350834.1:p.Arg145Gln
CA114727
NM_001363905.1:c.434G>A