Allele Registry

Canonical Allele Identifier: PA2827969200

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000215089

RCV000235925

RCV000271229

RCV002515673

RCV003947727

RCV003997982

ClinVar Variation:

232546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341827.1:p.Ser1817Thr	CA042221 NM_001354898.2:c.5449T>A