This allele is not present in the registry. To get a canonical identifier, please click on the "Get identifier" below.
Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
ENSP00000387483.2:p.Phe667Leu
ENST00000440126.7:c.1999T>C

ENST00000440126.7:c.2001T>A

ENST00000440126.7:c.2001T>G