Canonical Allele Identifier: PA1139677141
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 918313
ClinVar RCV Id: RCV002356818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp2044Asn
CA346002557
NM_000384.3:c.6130G>A