Canonical Allele Identifier: PA2828708379
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 68691
ClinVar RCV Id: RCV000059572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364208.1:p.Asn855Ile
CA219830
NM_001377279.1:c.2564A>T