Canonical Allele Identifier: PA214214
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36717
ClinVar RCV Id: RCV000030396 RCV000681591 RCV000788782 RCV001389165 RCV003407371 RCV003473150 RCV003991463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Trp416Leu
CA214212
NM_000536.4:c.1247G>T