Canonical Allele Identifier: PA2580114788
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1749691
ClinVar RCV Id: RCV002359799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu1933Ser
CA346003958
NM_000384.3:c.5798T>C