Canonical Allele Identifier: PA2828020200
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Glu1108Lys
CA008564
NM_001354903.2:c.3322G>A