Canonical Allele Identifier: PA2741817438
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2565868
ClinVar RCV Id: RCV003302093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Val4178Gly
CA345971033
NM_000384.3:c.12533T>G