Allele Registry

Canonical Allele Identifier: PA2827938989

Gene: PPARGC1A HGNC NCBI

ClinVar RCV:

RCV003976708

ClinVar Variation:

3056132

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341755.1:p.Thr485Met	CA2875162 NM_001354826.1:c.1454C>T