ClinGen Allele Registry
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Canonical Allele Identifier:
PA122869
Gene: RAG2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000014017
RCV000014018
RCV000681573
RCV003991458
ClinVar Variation:
13136
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000527.2:p.Arg39Gly
CA122867
NM_000536.4:c.115A>G