Allele Registry

Canonical Allele Identifier: PA915964322

Gene: APOB HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000231844

RCV000408839

RCV000494148

RCV000780859

RCV000844613

RCV001837444

RCV002243681

RCV002399350

RCV003147303

ClinVar Variation:

40223

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Arg3527Trp	CA044117 NM_000384.3:c.10579C>T