Canonical Allele Identifier: PA2828629278
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 378091
ClinVar RCV Id: RCV001000957 RCV001703462 RCV002263672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362738.1:p.Pro149Leu
CA8873555
NM_001375809.1:c.446C>T