Allele Registry

Canonical Allele Identifier: PA2828960856

Gene: APP HGNC NCBI

ClinVar Allele:

104133

ClinVar RCV:

RCV000084577

ClinVar Variation:

98241

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Leu667Pro	CA225513 NM_001385253.1:c.2000T>C