Canonical Allele Identifier: PA122856
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13130
ClinVar RCV Id: RCV000014010 RCV000014011 RCV000681586 RCV001049147 RCV001813982 RCV003398499 RCV003473086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Arg229Gln
CA122854
NM_000536.4:c.686G>A