Canonical Allele Identifier: PA2827964624
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met406Val
CA004131
NM_001354898.2:c.1216A>G