Canonical Allele Identifier: PA2830509016
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 897923
ClinVar RCV Id: RCV001141462
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958817.1:p.Lys650Asn
CA409805496
NM_201414.3:c.1950G>T
CA409805497
NM_201414.3:c.1950G>C