ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826270651
Gene: APP
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191231.1:p.Thr677Ala
CA127814
NM_001204302.2:c.2029A>G