Canonical Allele Identifier: PA2828707096
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364206.1:p.Arg975Trp
CA122919
NM_001377277.1:c.2923C>T