Canonical Allele Identifier: PA915963725
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 431493
ClinVar RCV Id: RCV000497133 RCV001138061 RCV001283876 RCV001142808 RCV001837931 RCV002438205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala990Thr
CA057625
NM_000384.3:c.2968G>A