Canonical Allele Identifier: PA2827938972
Gene: PPARGC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2541292
ClinVar RCV Id: RCV004309916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341755.1:p.Asp287Gly
CA356524776
NM_001354826.1:c.860A>G