Allele Registry

Canonical Allele Identifier: PA915963881

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000497190

RCV001508060

RCV001837933

ClinVar Variation:

431497

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Cys1422Tyr	CA43508675 NM_000384.3:c.4265G>A