Allele Registry

Canonical Allele Identifier: PA915964333

Gene: APOB HGNC NCBI

ClinVar Allele:

434171

ClinVar RCV:

RCV000508761

ClinVar Variation:

440521

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Glu3553Lys	CA044247 NM_000384.3:c.10657G>A