Allele Registry

Canonical Allele Identifier: PA915964339

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000019486

RCV000219069

RCV000412657

RCV000587550

RCV001837440

RCV002408470

ClinVar Variation:

17897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Arg3558Cys	CA022754 NM_000384.3:c.10672C>T