Canonical Allele Identifier: PA2830508764
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98235
ClinVar RCV Id: RCV000084559 RCV003430663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.His658Arg
CA225502
NM_201413.3:c.1973A>G