Canonical Allele Identifier: PA2825177113
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000439.2:p.Ser13Ala
CA5949891
NM_000448.3:c.37T>G