Canonical Allele Identifier: PA2828129707
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_001350917.1:p.Leu203Ser
CA396122257
NM_001363988.1:c.608T>C