Allele Registry

Canonical Allele Identifier: PA2827963699

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000199388

RCV000501209

RCV001270008

RCV001853212

ClinVar Variation:

216017

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341827.1:p.Arg116Ser	CA338613 NM_001354898.2:c.348G>T CA16022248 NM_001354898.2:c.348G>C