Canonical Allele Identifier: PA645493849
Gene: TNFSF12 HGNC NCBI

Linked Data

ClinVar Variation Id: 225690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003800.1:p.Arg145Cys
CA8350831
NM_003809.3:c.433C>T