Allele Registry

Canonical Allele Identifier: PA915963849

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV002487588

ClinVar Variation:

630135

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Arg1333Gly	CA060306 NM_000384.3:c.3997C>G