Canonical Allele Identifier: PA2825177709
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2951355
ClinVar RCV Id: RCV003805057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000439.2:p.Phe927Ser
CA380135290
NM_000448.3:c.2780T>C