Canonical Allele Identifier: PA2580115176
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2185701
ClinVar RCV Id: RCV002596279 RCV003161959
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg4177Gln
CA345971040
NM_000384.3:c.12530G>A