Allele Registry

Canonical Allele Identifier: PA2827998500

Gene: APC HGNC NCBI

ClinVar Variation Id: 1356107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341830.1:p.Ser2390Arg	CA16037325 NM_001354901.2:c.7168A>C CA16037331 NM_001354901.2:c.7170C>A CA16037332 NM_001354901.2:c.7170C>G