Canonical Allele Identifier: PA297669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1116Asp
CA008298
NM_000038.6:c.3347G>A