Allele Registry

Canonical Allele Identifier: PA210476

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000000839

RCV003743543

RCV003996070

ClinVar Variation:

802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Gly1120Glu	CA008319 NM_001127510.3:c.3359G>A