Canonical Allele Identifier: PA2827940792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Met431Val
CA004131
NM_001354895.2:c.1291A>G