Canonical Allele Identifier: PA1139695201
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959642
ClinVar RCV Id: RCV001233027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Leu240Pro
CA380142252
NM_001243786.2:c.719T>C