Canonical Allele Identifier: PA2827947499
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Met2491Val
CA048161
NM_001354895.2:c.7471A>G