Canonical Allele Identifier: PA2825869289
Gene: LIPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965942
ClinVar RCV Id: RCV002745398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138341.1:p.Gly156Arg
CA381976333
NM_001144869.3:c.466G>C
CA381976334
NM_001144869.3:c.466G>A