Canonical Allele Identifier: PA658671735
Gene: PLCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472906
ClinVar RCV Id: RCV000540341 RCV000768283 RCV001702518 RCV001336487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002652.2:p.Ala308Val
CA8193513
NM_002661.5:c.923C>T