ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA127807
Gene: APP
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000019729
RCV000084564
RCV000687111
ClinVar Variation:
18101
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191232.1:p.Asp601Asn
CA127804
NM_001204303.2:c.1801G>A