Canonical Allele Identifier: PA2573167271
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1355430
ClinVar RCV Id: RCV001866917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile1960Thr
CA346003777
NM_000384.3:c.5879T>C