Canonical Allele Identifier: PA915964146
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 477822
ClinVar RCV Id: RCV001837992 RCV003139868 RCV002377194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asn2961Ser
CA066085
NM_000384.3:c.8882A>G