Canonical Allele Identifier: PA2827975968
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1055767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly1092Arg
CA16028689
NM_001354899.2:c.3274G>A
CA16028690
NM_001354899.2:c.3274G>C