Allele Registry

Canonical Allele Identifier: PA115312

Gene: PPARGC1B HGNC NCBI

ClinVar RCV:

RCV000002119

RCV001534837

ClinVar Variation:

2039

HGVS (amino-acid)	Matching Registered Transcripts
NP_573570.3:p.Ala203Pro	CA115311 NM_133263.4:c.607G>C