Canonical Allele Identifier: PA2741817262
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2948657
ClinVar RCV Id: RCV003809431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu2458Lys
CA064354
NM_000384.3:c.7372G>A