Canonical Allele Identifier: PA2825193914
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046712
ClinVar RCV Id: RCV001351305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Ala136Val
CA380143213
NM_000536.4:c.407C>T