Canonical Allele Identifier: PA915964653
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334067
ClinVar RCV Id: RCV000303957 RCV000360983 RCV002480189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Tyr4534Cys
CA10614121
NM_000384.3:c.13601A>G