Canonical Allele Identifier: PA2828960844
Gene: APP HGNC NCBI
ClinVar RCV:
RCV000084571
ClinVar Variation:
98238
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.Val659Ala
CA225507
NM_001385253.1:c.1976T>C