Canonical Allele Identifier: PA2828629395
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 326646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362738.1:p.Pro378Ser
CA8873208
NM_001375809.1:c.1132C>T