Canonical Allele Identifier: PA916041616
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val2648Ile
CA014160
NM_001354896.2:c.7942G>A