Canonical Allele Identifier: PA2826270609
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2047418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Gly620Arg
CA409806585
NM_001204302.2:c.1858G>C
CA409806586
NM_001204302.2:c.1858G>A