Allele Registry

Canonical Allele Identifier: PA915964513

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000116381

RCV000256314

RCV000268700

RCV000771040

RCV001094720

RCV001837452

RCV002415597

ClinVar Variation:

128417

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Glu4181Lys	CA022778 NM_000384.3:c.12541G>A