Allele Registry

Canonical Allele Identifier: PA2828029154

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341832.1:p.Ser2480Arg	CA16038140 NM_001354903.2:c.7438A>C CA16038146 NM_001354903.2:c.7440T>A CA16038147 NM_001354903.2:c.7440T>G