Canonical Allele Identifier: PA2828028562
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Met2390Val
CA048161
NM_001354903.2:c.7168A>G