Canonical Allele Identifier: PA915963999
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 630628
ClinVar RCV Id: RCV001869110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Lys2240Thr
CA346000882
NM_000384.3:c.6719A>C