Canonical Allele Identifier: PA645509879
Gene: PLCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 440155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002652.2:p.His257Leu
CA8193451
NM_002661.5:c.770A>T