Canonical Allele Identifier: PA1139677022
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 926675
ClinVar RCV Id: RCV002491563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Val2007Met
CA062757
NM_000384.3:c.6019G>A