Canonical Allele Identifier: PA915963761
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 630322
ClinVar RCV Id: RCV002332560 RCV002535541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala1139Thr
CA058782
NM_000384.3:c.3415G>A