Allele Registry

Canonical Allele Identifier: PA1139714633

Gene: PLCG2 HGNC NCBI

ClinVar RCV:

RCV001204459

ClinVar Variation:

935795

HGVS (amino-acid)	Matching Registered Transcripts
NP_002652.2:p.Pro522Leu	CA396900063 NM_002661.5:c.1565C>T