Allele Registry

Canonical Allele Identifier: PA113492

Gene: LPL HGNC NCBI

ClinVar RCV:

RCV000001593

RCV001248903

RCV001388969

RCV003298025

ClinVar Variation:

1529

HGVS (amino-acid)	Matching Registered Transcripts
NP_000228.1:p.Ile221Thr	CA251867 NM_000237.3:c.662T>C