Canonical Allele Identifier: PA2580115180
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2189782
ClinVar RCV Id: RCV002611816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu4223Lys
CA345970734
NM_000384.3:c.12667G>A