Canonical Allele Identifier: PA2580115210
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1770675
ClinVar RCV Id: RCV002383332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu4520Ser
CA345967128
NM_000384.3:c.13559T>C