Allele Registry

Canonical Allele Identifier: PA2826270338

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019722

RCV000084557

RCV003509482

ClinVar Variation:

18095

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Glu647Asp	CA127797 NM_001204301.2:c.1941G>C CA409806514 NM_001204301.2:c.1941G>T