Allele Registry

Canonical Allele Identifier: PA915963629

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000116384

RCV000256290

RCV000295735

RCV000771026

RCV000845574

RCV001094640

RCV001837455

RCV002408617

ClinVar Variation:

128420

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Ala618Val	CA022801 NM_000384.3:c.1853C>T