Canonical Allele Identifier: PA915963752
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 252481
ClinVar RCV Id: RCV000238756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Lys1121Arg
CA10585965
NM_000384.3:c.3362A>G