Allele Registry

Canonical Allele Identifier: PA2828014417

Gene: APC HGNC NCBI

ClinVar Variation Id: 1764696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341835.1:p.Ser10Arg	CA16023234 NM_001354906.2:c.28A>C CA16023240 NM_001354906.2:c.30T>A CA16023241 NM_001354906.2:c.30T>G