Canonical Allele Identifier: PA916040941
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly2076Asp
CA010991
NM_001354896.2:c.6227G>A