Allele Registry

Canonical Allele Identifier: PA2827971626

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341827.1:p.Ser2556Arg	CA16038140 NM_001354898.2:c.7666A>C CA16038146 NM_001354898.2:c.7668T>A CA16038147 NM_001354898.2:c.7668T>G