Allele Registry

Canonical Allele Identifier: PA2827998940

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341830.1:p.Ser2522Arg	CA16038140 NM_001354901.2:c.7564A>C CA16038146 NM_001354901.2:c.7566T>A CA16038147 NM_001354901.2:c.7566T>G