Canonical Allele Identifier: PA2828127562
Gene: FTO HGNC NCBI

Linked Data

ClinVar Variation Id: 235247
ClinVar RCV Id: RCV000224338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350834.1:p.Arg284Ser
CA8058624
NM_001363905.1:c.852G>T
CA396123199
NM_001363905.1:c.852G>C