Canonical Allele Identifier: PA658831280
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 440231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Met502Val
CA5950404
NM_001243785.2:c.1504A>G