Canonical Allele Identifier: PA2580115215
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1770838
ClinVar RCV Id: RCV002383495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu4539Met
CA345966988
NM_000384.3:c.13615C>A