Canonical Allele Identifier: PA2827971322
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2466Val
CA048161
NM_001354898.2:c.7396A>G