Canonical Allele Identifier: PA2825177468
Gene: RAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 641796
ClinVar RCV Id: RCV000795118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000439.2:p.Phe520Ser
CA380152791
NM_000448.3:c.1559T>C