Canonical Allele Identifier: PA2825193997
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2622359
ClinVar RCV Id: RCV003381507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.His207Tyr
CA380142466
NM_000536.4:c.619C>T