Canonical Allele Identifier: PA915964247
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 218452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser3279Gly
CA066875
NM_000384.3:c.9835A>G