Canonical Allele Identifier: PA916027801
Gene: LIPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 438640
ClinVar RCV Id: RCV000505526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316871.1:p.Leu30Pro
CA224979330
NM_001329942.2:c.89T>C