Allele Registry

Canonical Allele Identifier: PA2828126790

Gene: FTO HGNC NCBI

ClinVar RCV:

RCV000190415

ClinVar Variation:

208336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350825.1:p.Ser319Phe	CA248803 NM_001363896.1:c.956C>T