Canonical Allele Identifier: PA2827981240
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_001341828.1:p.Met2685Ile
CA16039007
NM_001354899.2:c.8055G>A
CA16039008
NM_001354899.2:c.8055G>C
CA16039009
NM_001354899.2:c.8055G>T