Allele Registry

Canonical Allele Identifier: PA915964257

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000408877

RCV001256895

RCV001837890

RCV002411273

RCV003477905

ClinVar Variation:

369882

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Ala3354Gly	CA042354 NM_000384.3:c.10061C>G