Allele Registry

Canonical Allele Identifier: PA2825818932

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019716

RCV000084576

ClinVar Variation:

18090

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Val607Gly	CA127793 NM_001136131.2:c.1820T>G