Allele Registry

Canonical Allele Identifier: PA2828029021

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341835.1:p.Ser2298Arg	CA16038140 NM_001354906.2:c.6892A>C CA16038146 NM_001354906.2:c.6894T>A CA16038147 NM_001354906.2:c.6894T>G