Canonical Allele Identifier: PA2741817355
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2926213
ClinVar RCV Id: RCV003786499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser3282Gly
CA066885
NM_000384.3:c.9844A>G