Canonical Allele Identifier: PA2825177695
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13145
ClinVar RCV Id: RCV000014027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000439.2:p.Tyr912Cys
CA122892
NM_000448.3:c.2735A>G