Canonical Allele Identifier: PA2828629682
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 326632
ClinVar RCV Id: RCV000395862 RCV000480316 RCV002263038 RCV003950114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362738.1:p.Asp891Asn
CA8872637
NM_001375809.1:c.2671G>A