Canonical Allele Identifier: PA2826339116
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Arg229Gln
CA122854
NM_001243785.2:c.686G>A