Allele Registry

Canonical Allele Identifier: PA2825818936

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019733

RCV000518713

ClinVar Variation:

18105

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Val607Leu	CA127816 NM_001136131.2:c.1819G>C