Canonical Allele Identifier: PA2825177559
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 68689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000439.2:p.Arg699Trp
CA219824
NM_000448.3:c.2095C>T