Canonical Allele Identifier: PA915963994
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 808689
ClinVar RCV Id: RCV002249604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu2214Lys
CA346001236
NM_000384.3:c.6640G>A