Canonical Allele Identifier: PA915963763
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 237744
ClinVar RCV Id: RCV000456004 RCV000497223 RCV000771109 RCV000845457 RCV001137957 RCV002227096 RCV001837776 RCV002450671 RCV004529389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Pro1143Ser
CA058842
NM_000384.3:c.3427C>T