Canonical Allele Identifier: PA915963995
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg2219His
CA063423
NM_000384.3:c.6656G>A