Allele Registry

Canonical Allele Identifier: PA2825644589

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Ser2563Arg	CA16038140 NM_001127511.3:c.7687A>C CA16038146 NM_001127511.3:c.7689T>A CA16038147 NM_001127511.3:c.7689T>G