Canonical Allele Identifier: PA2826338727
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573475
ClinVar RCV Id: RCV000695159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Ile12Thr
CA5950633
NM_001243785.2:c.35T>C