Allele Registry

Canonical Allele Identifier: PA188052

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000163348

RCV000231340

RCV000758732

RCV000764565

RCV002267901

RCV003153439

RCV003995246

ClinVar Variation:

184169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Gly1702Glu	CA009865 NM_001127510.3:c.5105G>A