Allele Registry

Canonical Allele Identifier: PA2828126899

Gene: FTO HGNC NCBI

ClinVar RCV:

RCV000190415

ClinVar Variation:

208336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350826.1:p.Ser293Phe	CA248803 NM_001363897.1:c.878C>T