Canonical Allele Identifier: PA2828126757
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 884924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350825.1:p.Val201Ile
CA8058403
NM_001363896.1:c.601G>A