Canonical Allele Identifier: PA2828706468
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364206.1:p.Ser13Ala
CA5949891
NM_001377277.1:c.37T>G