Allele Registry

Canonical Allele Identifier: PA1139682830

Gene: APOB HGNC NCBI

ClinVar Allele:

260627

ClinVar RCV:

RCV000256307

RCV000845480

RCV001283874

RCV001837820

RCV002248497

RCV002379100

ClinVar Variation:

265896

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Gln4494del	CA1546518 NM_000384.3:c.13480_13482del