Canonical Allele Identifier: PA645511130
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 440231
ClinVar RCV Id: RCV000681604 RCV000645688 RCV001653875 RCV001103958 RCV001103959 RCV001579122 RCV000669183 RCV002282190 RCV003925510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Met502Val
CA5950404
NM_000536.4:c.1504A>G