Allele Registry

Canonical Allele Identifier: PA2828126978

Gene: FTO HGNC NCBI

ClinVar RCV:

RCV000398676

RCV000895438

ClinVar Variation:

319681

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350827.1:p.Ala134Thr	CA8058372 NM_001363898.1:c.400G>A