Canonical Allele Identifier: PA2828707158
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2079766
ClinVar RCV Id: RCV002998772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364207.1:p.Lys29Arg
CA5949900
NM_001377278.1:c.86A>G