Canonical Allele Identifier: PA2827988955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly2262Arg
CA012645
NM_001354900.2:c.6784G>A
CA16036399
NM_001354900.2:c.6784G>C