Allele Registry

Canonical Allele Identifier: PA2828012368

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341831.1:p.Ser2490Arg	CA16038140 NM_001354902.2:c.7468A>C CA16038146 NM_001354902.2:c.7470T>A CA16038147 NM_001354902.2:c.7470T>G