Canonical Allele Identifier: PA1139679980
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 927581
ClinVar RCV Id: RCV002375107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Val3273Ala
CA345988661
NM_000384.3:c.9818T>C