Canonical Allele Identifier: PA916019331
Gene: APOE HGNC NCBI

Linked Data

ClinVar Variation Id: 17848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289617.1:p.Arg202Cys
CA127498
NM_001302688.2:c.604C>T