Canonical Allele Identifier: PA1139744391
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 871801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364209.1:p.Arg716Trp
CA5950218
NM_001377280.1:c.2146C>T