Canonical Allele Identifier: PA2825808529
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18103
ClinVar RCV Id: RCV000019731 RCV000084565 RCV003987327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Leu681Val
CA127815
NM_001136016.3:c.2041C>G