Canonical Allele Identifier: PA2826339593
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000609
ClinVar RCV Id: RCV001296764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Pro501Ala
CA380140225
NM_001243785.2:c.1501C>G