Canonical Allele Identifier: PA645402319
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 235247
ClinVar RCV Id: RCV000224338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073901.1:p.Arg455Ser
CA8058624
NM_001080432.3:c.1365G>T
CA396123199
NM_001080432.3:c.1365G>C