Canonical Allele Identifier: PA915963764
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 265885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg1164Thr
CA058940
NM_000384.3:c.3491G>C