Canonical Allele Identifier: PA915964578
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 627769
ClinVar RCV Id: RCV001143333 RCV001141498 RCV001838139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile4341Asn
CA051712
NM_000384.3:c.13022T>A