Canonical Allele Identifier: PA2827466013
Gene: LPIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2183567
ClinVar RCV Id: RCV002627788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336130.1:p.Asp501His
CA345857868
NM_001349201.2:c.1501G>C