Canonical Allele Identifier: PA214217
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Glu437Lys
CA214215
NM_000536.4:c.1309G>A