Canonical Allele Identifier: PA658817132
Gene: PLCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540105
ClinVar RCV Id: RCV000650043
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Amino-acid Alleles

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