Canonical Allele Identifier: PA2825194027
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011251
ClinVar RCV Id: RCV001309016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Asn232Ser
CA5950539
NM_000536.4:c.695A>G