Canonical Allele Identifier: PA1139674820
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 925766
ClinVar RCV Id: RCV001644939 RCV002451393 RCV003770105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg1134Gly
CA058742
NM_000384.3:c.3400A>G