Allele Registry

Canonical Allele Identifier: PA2825818004

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084577

ClinVar Variation:

98241

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Leu592Pro	CA225513 NM_001136129.3:c.1775T>C