Allele Registry

Canonical Allele Identifier: PA225506

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084567

RCV001141463

ClinVar Variation:

98237

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Ala713Val	CA225505 NM_000484.4:c.2138C>T