Allele Registry

Canonical Allele Identifier: PA2825808487

Gene: APP HGNC NCBI

ClinVar Allele:

45806

ClinVar RCV:

RCV000030774

RCV000084558

RCV002513276

ClinVar Variation:

37145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Ala649Thr	CA130092 NM_001136016.3:c.1945G>A