Canonical Allele Identifier: PA1139680437
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 896639
ClinVar RCV Id: RCV001139433 RCV001139434 RCV003769666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr3428Asn
CA043011
NM_000384.3:c.10283C>A