Canonical Allele Identifier: PA916007314
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Asn474Ser
CA5950417
NM_001243786.2:c.1421A>G