Canonical Allele Identifier: PA2828127116
Gene: FTO HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350828.1:p.Arg278Gln
CA114727
NM_001363899.1:c.833G>A