Canonical Allele Identifier: PA916044581
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 235247
ClinVar RCV Id: RCV000224338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350832.1:p.Val414Leu
CA8058624
NM_001363903.1:c.1240G>T
CA396123199
NM_001363903.1:c.1240G>C