Allele Registry

Canonical Allele Identifier: PA2825818945

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001141462

ClinVar Variation:

897923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Lys615Asn	CA409805496 NM_001136131.2:c.1845G>T CA409805497 NM_001136131.2:c.1845G>C