Canonical Allele Identifier: PA2826339127
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2618577
ClinVar RCV Id: RCV003386338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Tyr234His
CA380142296
NM_001243785.2:c.700T>C