Canonical Allele Identifier: PA2580114845
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1754654
ClinVar RCV Id: RCV002366816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.His2215Gln
CA43505050
NM_000384.3:c.6645C>G
CA346001202
NM_000384.3:c.6645C>A