Canonical Allele Identifier: PA2741817259
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2681937
ClinVar RCV Id: RCV003477229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg2449Lys
CA43502707
NM_000384.3:c.7346G>A