Canonical Allele Identifier: PA2825818443
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18091
ClinVar RCV Id: RCV000019718 RCV000019717 RCV000020306 RCV000084561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Ala636Gly
CA127794
NM_001136130.2:c.1907C>G