Canonical Allele Identifier: PA2573187169
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1381133
ClinVar RCV Id: RCV001895213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Arg493Ile
CA380140273
NM_001243786.2:c.1478G>T