Canonical Allele Identifier: PA2826270614
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Glu628Asp
CA127797
NM_001204302.2:c.1884G>C
CA409806514
NM_001204302.2:c.1884G>T