Canonical Allele Identifier: PA2828012275
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met2331Val
CA048161
NM_001354905.2:c.6991A>G