Canonical Allele Identifier: PA1139682367
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 921861
ClinVar RCV Id: RCV002505767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Phe4284Ser
CA051347
NM_000384.3:c.12851T>C