Canonical Allele Identifier: PA2828628991
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362737.1:p.Leu504Phe
CA267513
NM_001375808.2:c.1510C>T