Allele Registry

Canonical Allele Identifier: PA2826339099

Gene: RAG2 HGNC NCBI

ClinVar RCV:

RCV001933482

ClinVar Variation:

1426815

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230714.1:p.Thr215Asn	CA5950547 NM_001243785.2:c.644C>A