Canonical Allele Identifier: PA916061935
Gene: TNFSF12-TNFSF13 HGNC NCBI

Linked Data

ClinVar Variation Id: 225690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742086.1:p.Arg145Cys
CA8350831
NM_172089.4:c.433C>T