Allele Registry

Canonical Allele Identifier: PA2580118026

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002926844

RCV003994471

ClinVar Variation:

2047418

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Gly657Arg	CA409806585 NM_000484.4:c.1969G>C CA409806586 NM_000484.4:c.1969G>A