Canonical Allele Identifier: PA2580201390
Gene: LIPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2039801
ClinVar RCV Id: RCV002886032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316870.1:p.Arg159Ser
CA600712358
NM_001329941.2:c.475C>A