Canonical Allele Identifier: PA2828126770
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 319684
ClinVar RCV Id: RCV000266601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350825.1:p.His261Gln
CA10648561
NM_001363896.1:c.783T>A
CA396119940
NM_001363896.1:c.783T>G