Canonical Allele Identifier: PA2580114794
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2451313
ClinVar RCV Id: RCV003182329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser1959Asn
CA346003785
NM_000384.3:c.5876G>A