Canonical Allele Identifier: PA2827976027
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1507413
ClinVar RCV Id: RCV003773388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu1108Gly
CA16028800
NM_001354899.2:c.3323A>G