Canonical Allele Identifier: PA2825194000
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 827734
ClinVar RCV Id: RCV001027617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Ile210Thr
CA380142446
NM_000536.4:c.629T>C