Allele Registry

Canonical Allele Identifier: PA2830508761

Gene: APP HGNC NCBI

ClinVar Allele:

45806

ClinVar RCV:

RCV000030774

RCV000084558

RCV002513276

ClinVar Variation:

37145

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Ala654Thr	CA130092 NM_201413.3:c.1960G>A