Canonical Allele Identifier: PA2580115027
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2003729
ClinVar RCV Id: RCV002811396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu3303Gln
CA066954
NM_000384.3:c.9907G>C