Allele Registry

Canonical Allele Identifier: PA658660119

Gene: APC HGNC NCBI

ClinVar Variation Id: 486737

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Gln1749His	CA16032805 NM_001127510.3:c.5247G>C CA16032806 NM_001127510.3:c.5247G>T