Canonical Allele Identifier: PA2828126407
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 522710
ClinVar RCV Id: RCV000625863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350820.1:p.Lys88Arg
CA396121503
NM_001363891.1:c.263A>G