Canonical Allele Identifier: PA2825808464
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Glu641Asp
CA127797
NM_001136016.3:c.1923G>C
CA409806514
NM_001136016.3:c.1923G>T