Canonical Allele Identifier: PA2828055646
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly956Asp
CA008298
NM_001354905.2:c.2867G>A