Canonical Allele Identifier: PA2741817404
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2531344
ClinVar RCV Id: RCV004301703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu3797Ile
CA345979270
NM_000384.3:c.11389T>A