Canonical Allele Identifier: PA2826339969
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3151193
ClinVar RCV Id: RCV004445582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230715.1:p.Gly190Val
CA380142573
NM_001243786.2:c.569G>T