Canonical Allele Identifier: PA2826270919
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18088
ClinVar RCV Id: RCV000019714 RCV000020308 RCV000084575 RCV003993747 RCV002496421
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Val624Ile
CA127791
NM_001204303.2:c.1870G>A