Canonical Allele Identifier: PA915963751
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 218443
ClinVar RCV Id: RCV000227119 RCV000247365 RCV000203119 RCV001137958 RCV001837749 RCV002321801 RCV000771075 RCV001094639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp1113His
CA058627
NM_000384.3:c.3337G>C