Canonical Allele Identifier: PA1139742280
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 888057
ClinVar RCV Id: RCV001121158 RCV002556606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350917.1:p.Asn143Ser
CA8058375
NM_001363988.1:c.428A>G