Allele Registry

Canonical Allele Identifier: PA916044577

Gene: FTO HGNC NCBI

ClinVar RCV:

RCV000190415

ClinVar Variation:

208336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350827.1:p.Ser329Phe	CA248803 NM_001363898.1:c.986C>T