Canonical Allele Identifier: PA113448
Gene: LPL HGNC NCBI

Linked Data

ClinVar Variation Id: 1522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000228.1:p.Gly215Glu
CA251861
NM_000237.3:c.644G>A