Canonical Allele Identifier: PA658817132
Gene: PLCG2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002652.2:p.Ala58Val
CA8193052
NM_002661.5:c.173C>T