Allele Registry

Canonical Allele Identifier: PA2827980797

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Ser2553Arg	CA16038140 NM_001354899.2:c.7657A>C CA16038146 NM_001354899.2:c.7659T>A CA16038147 NM_001354899.2:c.7659T>G