Allele Registry

Canonical Allele Identifier: PA2830508746

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002926844

RCV003994471

ClinVar Variation:

2047418

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Gly638Arg	CA409806585 NM_201413.3:c.1912G>C CA409806586 NM_201413.3:c.1912G>A