Canonical Allele Identifier: PA2826339503
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Trp453Arg
CA380140541
NM_001243785.2:c.1357T>C
CA380140542
NM_001243785.2:c.1357T>A