Canonical Allele Identifier: PA2826270923
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98241
ClinVar RCV Id: RCV000084577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Leu630Pro
CA225513
NM_001204303.2:c.1889T>C