Canonical Allele Identifier: PA2828960821
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18087
ClinVar RCV Id: RCV000019713 RCV001386879 RCV002272024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.Glu637Gln
CA127790
NM_001385253.1:c.1909G>C