Canonical Allele Identifier: PA2826270609
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2047418
ClinVar RCV Id: RCV002926844 RCV003994471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Gly620Arg
CA409806585
NM_001204302.2:c.1858G>C
CA409806586
NM_001204302.2:c.1858G>A