ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA127809
Gene: APP
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001129602.1:p.Asp638Asn
CA127804
NM_001136130.2:c.1912G>A