Canonical Allele Identifier: PA2828708309
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 950346
ClinVar RCV Id: RCV001222037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364208.1:p.Thr750Ser
CA380154311
NM_001377279.1:c.2248A>T
CA380154313
NM_001377279.1:c.2249C>G