Canonical Allele Identifier: PA645485206
Gene: LPL HGNC NCBI

Linked Data

ClinVar Variation Id: 424622
ClinVar RCV Id: RCV000487457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000228.1:p.Cys302Arg
CA16621522
NM_000237.3:c.904T>C