Canonical Allele Identifier: PA915963998
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 654490
ClinVar RCV Id: RCV001838224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile2233Thr
CA346000974
NM_000384.3:c.6698T>C