Canonical Allele Identifier: PA104348
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Gly451Ala
CA122872
NM_000536.4:c.1352G>C