Canonical Allele Identifier: PA915964559
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 801045
ClinVar RCV Id: RCV000985332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile4310Thr
CA43488346
NM_000384.3:c.12929T>C