Allele Registry

Canonical Allele Identifier: PA2826270923

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084577

ClinVar Variation:

98241

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Leu630Pro	CA225513 NM_001204303.2:c.1889T>C