Canonical Allele Identifier: PA2828126631
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 319681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350823.1:p.Ala134Thr
CA8058372
NM_001363894.1:c.400G>A