Canonical Allele Identifier: PA658827640
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496623
ClinVar RCV Id: RCV000681584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Tyr195Asp
CA380142545
NM_000536.4:c.583T>G