Allele Registry

Canonical Allele Identifier: PA2827973350

Gene: APC HGNC NCBI

ClinVar Variation Id: 1368407

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Ser262Arg	CA16023216 NM_001354899.2:c.784A>C CA16023221 NM_001354899.2:c.786T>A CA16023222 NM_001354899.2:c.786T>G