ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827914945
Gene: PPARG
HGNC
NCBI
Linked Data
ClinVar Variation Id:
8131
ClinVar RCV Id:
RCV000008604
RCV000008606
RCV000008605
RCV000008607
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341595.2:p.Pro10Ala
CA119314
NM_001354666.3:c.28C>G