Allele Registry

Canonical Allele Identifier: PA2825644184

Gene: APC HGNC NCBI

ClinVar Variation Id: 1356107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Ser2431Arg	CA16037325 NM_001127511.3:c.7291A>C CA16037331 NM_001127511.3:c.7293C>A CA16037332 NM_001127511.3:c.7293C>G