Allele Registry

Canonical Allele Identifier: PA2826270625

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Ala636Val	CA258118 NM_001204302.2:c.1907C>T