Canonical Allele Identifier: PA2826339031
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503410
ClinVar RCV Id: RCV002022809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Gly157Arg
CA380142925
NM_001243785.2:c.469G>A
CA380142928
NM_001243785.2:c.469G>C