Allele Registry

Canonical Allele Identifier: PA2828960853

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019716

RCV000084576

ClinVar Variation:

18090

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Val661Gly	CA127793 NM_001385253.1:c.1982T>G