Canonical Allele Identifier: PA2827998234
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly2311Val
CA046963
NM_001354901.2:c.6932G>T