Canonical Allele Identifier: PA2741817444
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2949042
ClinVar RCV Id: RCV003801768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu4271Gln
CA051272
NM_000384.3:c.12811G>C