Canonical Allele Identifier: PA2827277048
Gene: LIPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3119119
ClinVar RCV Id: RCV004407465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316870.1:p.Ile155Val
CA381976340
NM_001329941.2:c.463A>G