Canonical Allele Identifier: PA2580176986
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087899
ClinVar RCV Id: RCV003017966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Ile256Leu
CA380142158
NM_001243786.2:c.766A>C