Canonical Allele Identifier: PA2825194306
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1351921
ClinVar RCV Id: RCV002047210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Pro496Ser
CA380140258
NM_000536.4:c.1486C>T