ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA127813
Gene: APP
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001191230.1:p.Asp676Asn
NM_001204301.2:c.2026G>A