Canonical Allele Identifier: PA2826339501
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Gly451Ala
CA122872
NM_001243785.2:c.1352G>C