Canonical Allele Identifier: PA2741817357
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2941966
ClinVar RCV Id: RCV003802988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu3315Val
CA345988212
NM_000384.3:c.9943C>G