Canonical Allele Identifier: PA2828629207
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 326632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362737.1:p.Asp891Asn
CA8872637
NM_001375808.2:c.2671G>A