Canonical Allele Identifier: PA2825869285
Gene: LIPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1644695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138341.1:p.Pro139Ser
CA224979277
NM_001144869.3:c.415C>T