Allele Registry

Canonical Allele Identifier: PA916044607

Gene: FTO HGNC NCBI

ClinVar RCV:

RCV000398676

RCV000895438

ClinVar Variation:

319681

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350917.1:p.Ala134Thr	CA8058372 NM_001363988.1:c.400G>A