Canonical Allele Identifier: PA2828126993
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 1341534
ClinVar RCV Id: RCV001837050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350827.1:p.Leu203Ser
CA396122257
NM_001363898.1:c.608T>C