Canonical Allele Identifier: PA2825818466
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98237
ClinVar RCV Id: RCV000084567 RCV001141463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Ala657Val
CA225505
NM_001136130.2:c.1970C>T