Canonical Allele Identifier: PA915963755
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 695322
ClinVar RCV Id: RCV001838249 RCV002510992 RCV004029288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg1128Cys
CA058700
NM_000384.3:c.3382C>T