Allele Registry

Canonical Allele Identifier: PA2828032163

Gene: APC HGNC NCBI

ClinVar Variation Id: 1764696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341833.1:p.Ser268Arg	CA16023234 NM_001354904.2:c.802A>C CA16023240 NM_001354904.2:c.804T>A CA16023241 NM_001354904.2:c.804T>G