Canonical Allele Identifier: PA2828629106
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362737.1:p.Ser734Leu
CA340316
NM_001375808.2:c.2201C>T