Canonical Allele Identifier: PA2825869286
Gene: LIPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1954719
ClinVar RCV Id: RCV002690155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138341.1:p.Asp148Glu
CA381976385
NM_001144869.3:c.444C>A
CA381976386
NM_001144869.3:c.444C>G