Canonical Allele Identifier: PA1139677290
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 180280
ClinVar RCV Id: RCV000157119 RCV000181039 RCV000471850 RCV000776056 RCV001262209 RCV001837464 RCV002362835 RCV004535019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp2213del
CA022887
NM_000384.3:c.6639_6641del