Canonical Allele Identifier: PA2580114790
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2401887
ClinVar RCV Id: RCV004238772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Lys1947Arg
CA062533
NM_000384.3:c.5840A>G