Allele Registry

Canonical Allele Identifier: PA2830508748

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002653213

ClinVar Variation:

1937323

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Asn641Ser	CA409806564 NM_201413.3:c.1922A>G