Canonical Allele Identifier: PA2828013170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val2470Ile
CA014160
NM_001354905.2:c.7408G>A