Canonical Allele Identifier: PA645509880
Gene: PLCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 440158
ClinVar RCV Id: RCV000548599 RCV001573290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002652.2:p.Tyr482His
CA8193757
NM_002661.5:c.1444T>C