Allele Registry

Canonical Allele Identifier: PA2825635917

Gene: APC HGNC NCBI

ClinVar Variation Id: 1368407

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Ser290Arg	CA16023216 NM_001127510.3:c.868A>C CA16023221 NM_001127510.3:c.870T>A CA16023222 NM_001127510.3:c.870T>G