Canonical Allele Identifier: PA2573074406
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 641796
ClinVar RCV Id: RCV000795118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364209.1:p.Phe520Ser
CA380152791
NM_001377280.1:c.1559T>C