Allele Registry

Canonical Allele Identifier: PA113515

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019721

RCV000084566

RCV000547582

RCV000826088

RCV002272025

ClinVar Variation:

18094

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Ala713Thr	CA090906 NM_000484.4:c.2137G>A