Canonical Allele Identifier: PA2828126937
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 235247
ClinVar RCV Id: RCV000224338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350826.1:p.Arg429Ser
CA8058624
NM_001363897.1:c.1287G>T
CA396123199
NM_001363897.1:c.1287G>C