Allele Registry

Canonical Allele Identifier: PA2825014080

Gene: APC HGNC NCBI

ClinVar Variation Id: 1764696

HGVS (amino-acid)	Matching Registered Transcripts
NP_000029.2:p.Ser293Arg	CA16023234 NM_000038.6:c.877A>C CA16023240 NM_000038.6:c.879T>A CA16023241 NM_000038.6:c.879T>G