Canonical Allele Identifier: PA2828126674
Gene: FTO HGNC NCBI
ClinVar RCV:
RCV000001110
ClinVar Variation:
1055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350823.1:p.Arg316Gln
CA114727
NM_001363894.1:c.947G>A