Canonical Allele Identifier: PA297670
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly1116Asp
CA008298
NM_001127510.3:c.3347G>A