Canonical Allele Identifier: PA2828629466
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362738.1:p.Leu504Phe
CA267513
NM_001375809.1:c.1510C>T