Canonical Allele Identifier: PA2826918772
Gene: LIPG HGNC NCBI

Linked Data

ClinVar Variation Id: 2080567
ClinVar RCV Id: RCV002983138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294935.1:p.Val296Ile
CA8959301
NM_001308006.2:c.886G>A