Canonical Allele Identifier: PA915963969
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 430496
ClinVar RCV Id: RCV000494309 RCV003302730 RCV002481575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp1997Glu
CA062703
NM_000384.3:c.5991T>A
CA346003535
NM_000384.3:c.5991T>G