Canonical Allele Identifier: PA2825818945
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_001129603.1:p.Lys615Asn
CA409805496
NM_001136131.2:c.1845G>T
CA409805497
NM_001136131.2:c.1845G>C