Canonical Allele Identifier: PA2827938971
Gene: PPARGC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 788779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341755.1:p.Leu283Ile
CA2875283
NM_001354826.1:c.847C>A