Allele Registry

Canonical Allele Identifier: PA2826077393

Gene: PPARGC1B HGNC NCBI

ClinVar RCV:

RCV000002119

RCV001534837

ClinVar Variation:

2039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166170.1:p.Ala139Pro	CA115311 NM_001172699.2:c.415G>C