Canonical Allele Identifier: PA2826270623
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 37145
ClinVar RCV Id: RCV000030774 RCV000084558 RCV002513276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Ala636Thr
CA130092
NM_001204302.2:c.1906G>A