Canonical Allele Identifier: PA2825818449
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18098
ClinVar RCV Id: RCV000019725 RCV000020307 RCV000019726 RCV000084563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Glu637Gly
CA127801
NM_001136130.2:c.1910A>G