Canonical Allele Identifier: PA915964642
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 630176
ClinVar RCV Id: RCV002386346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp4522Asn
CA053193
NM_000384.3:c.13564G>A