Canonical Allele Identifier: PA658827641
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000527.2:p.Arg229Trp
CA5950542
NM_000536.4:c.685C>T