Allele Registry

Canonical Allele Identifier: PA915963466

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000313793

RCV000354570

RCV000604267

RCV000759460

RCV001094746

RCV001837882

RCV002328858

ClinVar Variation:

334184

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Pro145Ser	CA060888 NM_000384.3:c.433C>T