Allele Registry

Canonical Allele Identifier: PA915963812

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000256241

RCV000524085

RCV000532315

RCV001027453

RCV001140852

RCV001837813

RCV002365272

RCV004535240

ClinVar Variation:

265886

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Tyr1247Cys	CA059556 NM_000384.3:c.3740A>G