Allele Registry

Canonical Allele Identifier: PA113579

Gene: LPL HGNC NCBI

ClinVar RCV:

RCV000001616

ClinVar Variation:

1551

HGVS (amino-acid)	Matching Registered Transcripts
NP_000228.1:p.Leu392Val	CA251888 NM_000237.3:c.1174C>G