Canonical Allele Identifier: PA2826338775
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2922184
ClinVar RCV Id: RCV003785398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Gly35Ser
CA380144633
NM_001243785.2:c.103G>A