Allele Registry

Canonical Allele Identifier: PA2828048498

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341833.1:p.Ser2455Arg	CA16038140 NM_001354904.2:c.7363A>C CA16038146 NM_001354904.2:c.7365T>A CA16038147 NM_001354904.2:c.7365T>G