Canonical Allele Identifier: PA1139677282
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 404406
ClinVar RCV Id: RCV001837911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp2203del
CA16610674
NM_000384.3:c.6609_6611del