Canonical Allele Identifier: PA915964015
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 627652
ClinVar RCV Id: RCV001142363 RCV001140519 RCV001838134 RCV004027231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile2310Thr
CA063773
NM_000384.3:c.6929T>C