Canonical Allele Identifier: PA2827980494
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met2463Val
CA048161
NM_001354899.2:c.7387A>G