Canonical Allele Identifier: PA658827650
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496633
ClinVar RCV Id: RCV000681601 RCV001247197 RCV001834863 RCV003492116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Asn474Ser
CA5950417
NM_000536.4:c.1421A>G