Allele Registry

Canonical Allele Identifier: PA2825818836

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002926844

RCV003994471

ClinVar Variation:

2047418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Gly547Arg	CA409806585 NM_001136131.2:c.1639G>C CA409806586 NM_001136131.2:c.1639G>A