Allele Registry

Canonical Allele Identifier: PA113581

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084577

ClinVar Variation:

98241

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Leu723Pro	CA225513 NM_000484.4:c.2168T>C