Canonical Allele Identifier: PA2580114847
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2446989
ClinVar RCV Id: RCV003164967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.His2230Tyr
CA063446
NM_000384.3:c.6688C>T