Canonical Allele Identifier: PA2826873750
Gene: APOE HGNC NCBI

Linked Data

ClinVar Variation Id: 17876
ClinVar RCV Id: RCV000019462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289620.1:p.Ser314Arg
CA127521
NM_001302691.2:c.940A>C
CA406306024
NM_001302691.2:c.942C>A
CA406306025
NM_001302691.2:c.942C>G