Canonical Allele Identifier: PA2828126415
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 319681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350820.1:p.Ala134Thr
CA8058372
NM_001363891.1:c.400G>A