Canonical Allele Identifier: PA2826918736
Gene: LIPG HGNC NCBI

Linked Data

ClinVar Variation Id: 1942660
ClinVar RCV Id: RCV002646914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294935.1:p.Met94Ile
CA402418376
NM_001308006.2:c.282G>A
CA402418377
NM_001308006.2:c.282G>C
CA402418378
NM_001308006.2:c.282G>T