Canonical Allele Identifier: PA1139744398
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 256189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364209.1:p.Lys820Arg
CA5950267
NM_001377280.1:c.2459A>G