Canonical Allele Identifier: PA2826338773
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Gly35Ala
CA214209
NM_001243785.2:c.104G>C