Canonical Allele Identifier: PA2827972070
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827477
ClinVar Variation Id: 1762143
ClinVar RCV Id: RCV002421348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2688Ile
CA16039007
NM_001354898.2:c.8064G>A
CA16039008
NM_001354898.2:c.8064G>C
CA16039009
NM_001354898.2:c.8064G>T