Canonical Allele Identifier: PA2826338838
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 427020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Asp65Tyr
CA380144219
NM_001243785.2:c.193G>T