Canonical Allele Identifier: PA1139682272
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 925122
ClinVar RCV Id: RCV002418635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.His4183Arg
CA050535
NM_000384.3:c.12548A>G