Allele Registry

Canonical Allele Identifier: PA2827973363

Gene: APC HGNC NCBI

ClinVar Variation Id: 1764696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Ser265Arg	CA16023234 NM_001354899.2:c.793A>C CA16023240 NM_001354899.2:c.795T>A CA16023241 NM_001354899.2:c.795T>G