Canonical Allele Identifier: PA2828126844
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 522710
ClinVar RCV Id: RCV000625863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350826.1:p.Lys62Arg
CA396121503
NM_001363897.1:c.185A>G