Canonical Allele Identifier: PA2499231921
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1008170
ClinVar RCV Id: RCV001838480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.His2215Asn
CA346001212
NM_000384.3:c.6643C>A