Canonical Allele Identifier: PA122869
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Arg39Gly
CA122867
NM_000536.4:c.115A>G