Canonical Allele Identifier: PA2826270890
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2628367
ClinVar RCV Id: RCV003397222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Lys594Asn
CA409806220
NM_001204303.2:c.1782A>T
CA409806222
NM_001204303.2:c.1782A>C