Allele Registry

Canonical Allele Identifier: PA915964617

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV001138900

RCV001138901

RCV001256751

RCV001283873

RCV001837970

RCV002384270

RCV004543254

ClinVar Variation:

477800

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Asp4457Asn	CA052562 NM_000384.3:c.13369G>A