Canonical Allele Identifier: PA2825869287
Gene: LIPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1940508
ClinVar RCV Id: RCV002639369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138341.1:p.Asp149His
CA381976383
NM_001144869.3:c.445G>C