Allele Registry

Canonical Allele Identifier: PA915964040

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000581160

RCV004017684

RCV004024626

ClinVar Variation:

490400

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Lys2428Arg	CA345997492 NM_000384.3:c.7283A>G