Allele Registry

Canonical Allele Identifier: PA2741868098

Gene: PPARGC1A HGNC NCBI

ClinVar RCV:

RCV003976708

ClinVar Variation:

3056132

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341756.1:p.Thr617Met	CA2875162 NM_001354827.2:c.1850C>T