Canonical Allele Identifier: PA2826339515
Gene: RAG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496632
ClinVar RCV Id: RCV000681600 RCV001378887 RCV001834862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230714.1:p.Met459Leu
CA380140499
NM_001243785.2:c.1375A>C
CA380140500
NM_001243785.2:c.1375A>T