Canonical Allele Identifier: PA1139677246
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 933432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp2162Asn
CA063273
NM_000384.3:c.6484G>A