Canonical Allele Identifier: PA297745
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met431Val
CA004131
NM_001127510.3:c.1291A>G