Canonical Allele Identifier: PA2827968736
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1678Arg
CA16032494
NM_001354898.2:c.5032G>A
CA16032495
NM_001354898.2:c.5032G>C