Canonical Allele Identifier: PA2825194034
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 965599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Leu240Phe
CA5950537
NM_000536.4:c.718C>T