Canonical Allele Identifier: PA2580115214
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2140081
ClinVar RCV Id: RCV003066755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu4539Pro
CA053357
NM_000384.3:c.13616T>C