Canonical Allele Identifier: PA122866
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13135
ClinVar RCV Id: RCV000014016 RCV000433357 RCV000681585 RCV000645697 RCV001081978 RCV001104047 RCV001104048 RCV003492295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Thr215Ile
CA122864
NM_000536.4:c.644C>T