Allele Registry

Canonical Allele Identifier: PA2827953332

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341825.1:p.Ser2599Arg	CA16038140 NM_001354896.2:c.7795A>C CA16038146 NM_001354896.2:c.7797T>A CA16038147 NM_001354896.2:c.7797T>G