Allele Registry

Canonical Allele Identifier: PA2828127119

Gene: FTO HGNC NCBI

ClinVar RCV:

RCV000190415

ClinVar Variation:

208336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350828.1:p.Ser281Phe	CA248803 NM_001363899.1:c.842C>T