Canonical Allele Identifier: PA2828127097
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 884924
ClinVar RCV Id: RCV001116238 RCV001862894 RCV002558147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350828.1:p.Val201Ile
CA8058403
NM_001363899.1:c.601G>A