Allele Registry

Canonical Allele Identifier: PA2827941844

Gene: APC HGNC NCBI

ClinVar Variation Id: 469744

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341824.1:p.Ser787Gly	CA031761 NM_001354895.2:c.2359A>G