Canonical Allele Identifier: PA1139680327
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 927807
ClinVar RCV Id: RCV002379737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser3415Thr
CA042839
NM_000384.3:c.10244G>C