Canonical Allele Identifier: PA2827347137
Gene: PPARGC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2541292
ClinVar RCV Id: RCV004309916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317682.1:p.Asp287Gly
CA356524776
NM_001330753.2:c.860A>G