Canonical Allele Identifier: PA214211
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36716
ClinVar RCV Id: RCV000030395 RCV000681571 RCV000819784 RCV003137544 RCV003473149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Gly35Ala
CA214209
NM_000536.4:c.104G>C