Canonical Allele Identifier: PA2828628920
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 326646
ClinVar RCV Id: RCV000312207 RCV000482609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362737.1:p.Pro378Ser
CA8873208
NM_001375808.2:c.1132C>T