Canonical Allele Identifier: PA2828047838
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.His2370Gln
CA16037618
NM_001354904.2:c.7110T>A
CA16037619
NM_001354904.2:c.7110T>G