Canonical Allele Identifier: PA2828707137
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2116610
ClinVar RCV Id: RCV003024805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364206.1:p.Asp1033Gly
CA5950370
NM_001377277.1:c.3098A>G