Allele Registry

Canonical Allele Identifier: PA2828042742

Gene: APC HGNC NCBI

ClinVar Variation Id: 486737

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341833.1:p.Gln1623His	CA16032805 NM_001354904.2:c.4869G>C CA16032806 NM_001354904.2:c.4869G>T