Canonical Allele Identifier: PA2828127442
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 1341534
ClinVar RCV Id: RCV001837050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350832.1:p.Leu203Ser
CA396122257
NM_001363903.1:c.608T>C