Canonical Allele Identifier: PA2825194059
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087899
ClinVar RCV Id: RCV003017966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Ile256Leu
CA380142158
NM_000536.4:c.766A>C