Allele Registry

Canonical Allele Identifier: PA2825818871

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Lys577Asn	CA409806220 NM_001136131.2:c.1731A>T CA409806222 NM_001136131.2:c.1731A>C