Canonical Allele Identifier: PA2573062428
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1341571
ClinVar RCV Id: RCV001837067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gln1149Arg
CA346009070
NM_000384.3:c.3446A>G