Canonical Allele Identifier: PA2825635453
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_001120982.1:p.Met2713Ile
CA16039007
NM_001127510.3:c.8139G>A
CA16039008
NM_001127510.3:c.8139G>C
CA16039009
NM_001127510.3:c.8139G>T