Canonical Allele Identifier: PA2826270872
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Glu572Asp
CA127797
NM_001204303.2:c.1716G>C
CA409806514
NM_001204303.2:c.1716G>T