Canonical Allele Identifier: PA2827982882
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met372Val
CA004131
NM_001354900.2:c.1114A>G