Canonical Allele Identifier: PA2826270382
Gene: APP HGNC NCBI
ClinVar RCV:
RCV003223103
ClinVar Variation:
2498894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Ile698Phe
CA409805555
NM_001204301.2:c.2092A>T