Canonical Allele Identifier: PA2830508963
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958817.1:p.Glu590Asp
CA127797
NM_201414.3:c.1770G>C
CA409806514
NM_201414.3:c.1770G>T