Allele Registry

Canonical Allele Identifier: PA2830508981

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Lys612Asn	CA409806220 NM_201414.3:c.1836A>T CA409806222 NM_201414.3:c.1836A>C