ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2826270912
Gene: APP
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000019724
RCV000084570
RCV003509483
ClinVar Variation:
18097
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191232.1:p.Val622Met
CA127800
NM_001204303.2:c.1864G>A