Canonical Allele Identifier: PA2826270653
Gene: APP HGNC NCBI
ClinVar RCV:
RCV000084571
ClinVar Variation:
98238
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Val678Ala
CA225507
NM_001204302.2:c.2033T>C