Canonical Allele Identifier: PA2826270879
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 1315088
ClinVar RCV Id: RCV001773282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Met578Leu
CA319103456
NM_001204303.2:c.1732A>T
CA409806447
NM_001204303.2:c.1732A>C