Canonical Allele Identifier: PA915963964
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 548062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Val1955Met
CA062567
NM_000384.3:c.5863G>A