Allele Registry

Canonical Allele Identifier: PA2828012845

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341834.1:p.Ser2421Arg	CA16038140 NM_001354905.2:c.7261A>C CA16038146 NM_001354905.2:c.7263T>A CA16038147 NM_001354905.2:c.7263T>G