Canonical Allele Identifier: PA2826339426
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Trp416Leu
CA214212
NM_001243785.2:c.1247G>T