Canonical Allele Identifier: PA2825149507
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3127930
ClinVar RCV Id: RCV004417763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Lys3321Gln
CA345988147
NM_000384.3:c.9961A>C