Canonical Allele Identifier: PA916007254
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Thr215Ile
CA122864
NM_001243786.2:c.644C>T