Allele Registry

Canonical Allele Identifier: PA2579933931

Gene: APP HGNC NCBI

MaveDb:

Score 0.0116215858

Score 0.0637609662

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Lys687Asn	CA409806220 NM_000484.4:c.2061A>T CA409806222 NM_000484.4:c.2061A>C