Canonical Allele Identifier: PA2825194058
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035768
ClinVar RCV Id: RCV001338682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Gly255Val
CA380142160
NM_000536.4:c.764G>T