Canonical Allele Identifier: PA915964141
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 490402
ClinVar RCV Id: RCV000775483 RCV002377202 RCV001838002 RCV003478309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg2907His
CA065935
NM_000384.3:c.8720G>A