Canonical Allele Identifier: PA2579933593
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000475.1:p.Phe691Leu
NM_000484.4:c.2071T>C

NM_000484.4:c.2073T>A

NM_000484.4:c.2073T>G