Canonical Allele Identifier: PA2825635098
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His2496Gln
CA16037618
NM_001127510.3:c.7488T>A
CA16037619
NM_001127510.3:c.7488T>G