Canonical Allele Identifier: PA2825194028
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2618577
ClinVar RCV Id: RCV003386338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Tyr234His
CA380142296
NM_000536.4:c.700T>C