Canonical Allele Identifier: PA1139695200
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 849651
ClinVar RCV Id: RCV001053661 RCV001832489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Arg237Ser
CA380142269
NM_001243786.2:c.711G>T
CA380142270
NM_001243786.2:c.711G>C