Allele Registry

Canonical Allele Identifier: PA2828960765

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002926844

RCV003994471

ClinVar Variation:

2047418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Gly601Arg	CA409806585 NM_001385253.1:c.1801G>C CA409806586 NM_001385253.1:c.1801G>A