Canonical Allele Identifier: PA2828029070
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760236
ClinVar RCV Id: RCV002400612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2468Thr
CA16038070
NM_001354903.2:c.7403G>C