Canonical Allele Identifier: PA2828707034
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 68692
ClinVar RCV Id: RCV000059573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364206.1:p.Leu885Arg
CA219833
NM_001377277.1:c.2654T>G