Canonical Allele Identifier: PA2828028437
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Met2208Val
CA048161
NM_001354906.2:c.6622A>G