ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579933691
Gene: APP
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000475.1:p.Ile703Thr
CA409805623
NM_000484.4:c.2108T>C