Allele Registry

Canonical Allele Identifier: PA113635

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019733

RCV000518713

ClinVar Variation:

18105

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Val717Leu	CA127816 NM_000484.4:c.2149G>C