Canonical Allele Identifier: PA645479703
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 427020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Asp65Tyr
CA380144219
NM_000536.4:c.193G>T