Canonical Allele Identifier: PA1139744402
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 877627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364209.1:p.Arg829Ser
CA5950270
NM_001377280.1:c.2487G>T
CA380154830
NM_001377280.1:c.2487G>C