Canonical Allele Identifier: PA915964290
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 627775
ClinVar RCV Id: RCV001192835 RCV001838142 RCV002388392 RCV004540091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Tyr3462Cys
CA043373
NM_000384.3:c.10385A>G