Canonical Allele Identifier: PA267515
Gene: LPIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97814
ClinVar RCV Id: RCV000084067 RCV000221897 RCV000762223 RCV002262674 RCV003915108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055461.1:p.Leu504Phe
CA267513
NM_014646.2:c.1510C>T