Canonical Allele Identifier: PA915964016
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 128424
ClinVar Variation Id: 1168905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile2313Val
CA063826
NM_000384.3:c.6937A>G
CA43504666
NM_000384.3:c.6936_6937delinsTG