Allele Registry

Canonical Allele Identifier: PA2825817998

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019733

RCV000518713

ClinVar Variation:

18105

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Val586Leu	CA127816 NM_001136129.3:c.1756G>C