Canonical Allele Identifier: PA2573187074
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1447627
ClinVar RCV Id: RCV002011950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Val247Glu
CA380142210
NM_001243786.2:c.740T>A