Allele Registry

Canonical Allele Identifier: PA2830508996

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084567

RCV001141463

ClinVar Variation:

98237

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Ala638Val	CA225505 NM_201414.3:c.1913C>T