Allele Registry

Canonical Allele Identifier: PA2830508788

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019728

RCV000084569

ClinVar Variation:

18100

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Thr695Ile	CA127803 NM_201413.3:c.2084C>T