Canonical Allele Identifier: PA2741817459
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2923518
ClinVar RCV Id: RCV003783076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr4560Asn
CA053475
NM_000384.3:c.13679C>A