Canonical Allele Identifier: PA915964324
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 17890
ClinVar RCV Id: RCV000019479 RCV000254882 RCV000412515 RCV000499833 RCV000771116 RCV000844612 RCV000851289 RCV001837437 RCV002399330 RCV002287339 RCV004528126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg3527Gln
CA022750
NM_000384.3:c.10580G>A