Canonical Allele Identifier: PA915964250
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 544097
ClinVar RCV Id: RCV001838045 RCV001335284 RCV001584512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu3313Ile
CA066985
NM_000384.3:c.9937C>A