Canonical Allele Identifier: PA2826270666
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98242
ClinVar RCV Id: RCV000084578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Lys687Asn
CA225514
NM_001204302.2:c.2061G>C
CA409805504
NM_001204302.2:c.2061G>T