Canonical Allele Identifier: PA2827980514
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His2468Gln
CA16037618
NM_001354899.2:c.7404T>A
CA16037619
NM_001354899.2:c.7404T>G