Canonical Allele Identifier: PA342169
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 21520
ClinVar RCV Id: RCV000020710 RCV000755296 RCV002262570 RCV003982845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055461.1:p.Ala331Ser
CA342167
NM_014646.2:c.991G>T