Canonical Allele Identifier: PA2828629368
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 21520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362738.1:p.Ala331Ser
CA342167
NM_001375809.1:c.991G>T