Canonical Allele Identifier: PA915963727
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 237743
ClinVar RCV Id: RCV000256285 RCV000454922 RCV000766983 RCV001142806 RCV001142807 RCV001837775 RCV002433954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Pro994Leu
CA057651
NM_000384.3:c.2981C>T