Canonical Allele Identifier: PA2827989147
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly2321Ala
CA16036765
NM_001354900.2:c.6962G>C