Allele Registry

Canonical Allele Identifier: PA915964323

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV000508958

ClinVar Variation:

440523

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Arg3527Leu	CA345986090 NM_000384.3:c.10580G>T