Canonical Allele Identifier: PA2827998636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met2432Val
CA048161
NM_001354901.2:c.7294A>G