Allele Registry

Canonical Allele Identifier: PA915964264

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000157117

ClinVar Variation:

180278

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Ala3396Asp	CA022739 NM_000384.3:c.10187C>A