Canonical Allele Identifier: PA915964529
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 255976
ClinVar RCV Id: RCV000245435 RCV000370304 RCV000434263 RCV001094662 RCV001837796 RCV002374414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser4233Thr
CA050895
NM_000384.3:c.12697T>A