ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830508779
Gene: APP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
18103
ClinVar RCV Id:
RCV000019731
RCV000084565
RCV003987327
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_958816.1:p.Leu686Val
CA127815
NM_201413.3:c.2056C>G