Canonical Allele Identifier: PA2826270391
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 897923
ClinVar RCV Id: RCV001141462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Lys707Asn
CA409805496
NM_001204301.2:c.2121G>T
CA409805497
NM_001204301.2:c.2121G>C