Canonical Allele Identifier: PA915963996
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 402377
ClinVar RCV Id: RCV000454449 RCV001284264 RCV001861656 RCV002365577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg2219Cys
CA063418
NM_000384.3:c.6655C>T