Canonical Allele Identifier: PA915964041
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 218448
ClinVar RCV Id: RCV000203158 RCV000224080 RCV000771126 RCV001139737 RCV002381696 RCV000417323 RCV000456013 RCV001139738 RCV001837754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser2429Thr
CA064271
NM_000384.3:c.7285T>A