Canonical Allele Identifier: PA2741839894
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2622359
ClinVar RCV Id: RCV003381507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.His207Tyr
CA380142466
NM_001243786.2:c.619C>T