Canonical Allele Identifier: PA1139742250
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 884924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350834.1:p.Val30Ile
CA8058403
NM_001363905.1:c.88G>A