Canonical Allele Identifier: PA2826918725
Gene: LIPG HGNC NCBI

Linked Data

ClinVar Variation Id: 1169605
ClinVar RCV Id: RCV001521111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294935.1:p.Gly26Ser
CA8958968
NM_001308006.2:c.76G>A