Allele Registry

Canonical Allele Identifier: PA2827979850

Gene: APC HGNC NCBI

ClinVar Variation Id: 644645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Ser2267Ala	CA16036352 NM_001354899.2:c.6799T>G