Canonical Allele Identifier: PA2828126862
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 445384
ClinVar RCV Id: RCV000514150 RCV001116237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350826.1:p.Gly156Ala
CA8058392
NM_001363897.1:c.467G>C