Allele Registry

Canonical Allele Identifier: PA2828023061

Gene: APC HGNC NCBI

ClinVar Variation Id: 350413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341835.1:p.Phe1401Leu	CA10618781 NM_001354906.2:c.4201T>C CA16032379 NM_001354906.2:c.4203T>A CA16032380 NM_001354906.2:c.4203T>G