Canonical Allele Identifier: PA2827940246
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp256Glu
CA16023011
NM_001354895.2:c.768T>A
CA16023012
NM_001354895.2:c.768T>G