Allele Registry

Canonical Allele Identifier: PA645401999

Gene: APC HGNC NCBI

ClinVar Allele:

406586

ClinVar RCV:

RCV000479194

RCV002367649

RCV003766710

ClinVar Variation:

422747

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Ser2343Phe	CA16036653 NM_001127510.3:c.7028C>T