Allele Registry

Canonical Allele Identifier: PA167921

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000131289

RCV002228321

ClinVar Variation:

142268

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Val1463Ile	CA009548 NM_001127511.3:c.4387G>A