Canonical Allele Identifier: PA2826338996
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1022035
ClinVar RCV Id: RCV001321894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Val145Ala
CA380143089
NM_001243785.2:c.434T>C