Canonical Allele Identifier: PA2580115206
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1770192
ClinVar RCV Id: RCV002387540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.His4445Pro
CA345967633
NM_000384.3:c.13334A>C