Allele Registry

Canonical Allele Identifier: PA645464236

Gene: PLCG2 HGNC NCBI

ClinVar Variation Id: 432319

HGVS (amino-acid)	Matching Registered Transcripts
NP_002652.2:p.Thr168Ala	CA8193249 NM_002661.5:c.502A>G