Allele Registry

Canonical Allele Identifier: PA156808

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000120032

RCV000131590

RCV000587624

RCV001153055

RCV003323291

ClinVar Variation:

133522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Ser2497Leu	CA013717 NM_001127510.3:c.7490C>T