Allele Registry

Canonical Allele Identifier: PA2825818922

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019723

RCV000084573

RCV001947096

ClinVar Variation:

18096

1457308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Ile606Val	CA127799 NM_001136131.2:c.1816A>G CA2573157339 NM_001136131.2:c.1815_1816delinsTG