Canonical Allele Identifier: PA2828126425
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 445384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350820.1:p.Gly182Ala
CA8058392
NM_001363891.1:c.545G>C